Disease Browser
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Parent Node: Ataxia (D001259) |
Parent Node: Growth Disorders (D006130) |
Parent Node: Hearing Loss (D034381) |
Parent Node: Intellectual Disability (D008607) |
..Starting node ..Reardon Wilson Cavanagh syndrome (C535295)
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Child Nodes:
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Sister Nodes: |
..15q24 Microdeletion (C579849)
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..16p11.2 Deletion Syndrome (C579850)
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..Absent Eyebrows and Eyelashes with Mental Retardation (C563111)
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..Acrodysostosis (C538179)
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..Agonadism, XY, with Mental Retardation, Short Stature, Retarded Bone Age, and Multiple Extragenital Malformations (C563429)
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..AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency (C563876)
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..Akesson syndrome (C535610)
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..Al Gazali Aziz Salem syndrome (C535613)
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..Alaninuria with Microcephaly, Dwarfism, Enamel Hypoplasia, and Diabetes Mellitus (C565968)
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..Alopecia contractures dwarfism mental retardation (C537051)
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..Alopecia epilepsy oligophrenia syndrome of Moynahan (C537052)
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..Alopecia, epilepsy, pyorrhea, mental subnormality (C537057)
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..Alopecia, Neurologic Defects, and Endocrinopathy Syndrome (C567425)
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..Alopecia-Mental Retardation Syndrome 1 (C565965)
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..Alopecia-Mental Retardation Syndrome 2 (C563668)
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..ALOPECIA-MENTAL RETARDATION SYNDROME 3 (OMIM:613930)
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..Alopecia-Mental Retardation Syndrome with Convulsions and Hypergonadotropic Hypogonadism (C563370)
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..Alpha-Thalassemia Mental Retardation Syndrome, Deletion-Type (C563050)
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..Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis (C564570)
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..Amino Aciduria with Mental Deficiency, Dwarfism, Muscular Dystrophy, Osteoporosis, and Acidosis (C565960)
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..Amyloidosis of Gingiva and Conjunctiva, with Mental Retardation (C565958)
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..Amyotrophic Dystonic Paraplegia (C566292)
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..Anemia, Congenital Hypoplastic, with Multiple Congenital Anomalies/Mental Retardation Syndrome (C565796)
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..Aniridia cerebellar ataxia mental deficiency (C536370)
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..Ansell Bywaters Elderking syndrome (C537773)
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..Aortic arch anomaly with peculiar facies and mental retardation (C537785)
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..Aphalangia, Partial, with Syndactyly and Duplication of Metatarsal IV (C563942)
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..Arachnodactyly ataxia cataract aminoaciduria mental retardation (C537424)
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..Arginine:Glycine Amidinotransferase Deficiency (C567192)
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..Arthrogryposis, distal, with hypopituitarism, mental retardation, and facial anomalies (C535385)
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..Arthrogryposis, Distal, with Mental Retardation and Characteristic Facies (C565940)
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..Aughton syndrome (C538269)
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..Aural Atresia, Multiple Congenital Anomalies, and Mental Retardation (C565923)
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..Baraitser Rodeck Garner syndrome (C537906)
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..Battaglia Neri syndrome (C537662)
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..BEAULIEU-BOYCOTT-INNES SYNDROME (OMIM:613680)
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..Behr syndrome (C537669)
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..Bellini Chiumello Rimoldi syndrome (C535652)
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..Biemond Syndrome II (C565902)
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..Biemond syndrome type 2 (C535439)
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..Birk-Barel Mental Retardation Dysmorphism Syndrome (C567357)
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..Blepharophimosis syndrome Ohdo type (C536232)
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..Blepharophimosis with Facial and Genital Anomalies and Mental Retardation (C565797)
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..Bohring syndrome (C537419)
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..Boudhina Yedes Khiari syndrome (C537939)
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..BRACHYDACTYLY-MENTAL RETARDATION SYNDROME (OMIM:600430)
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..Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear/Eye Anomalies, Cleft Palate/Cryptorchidism, And (C564519)
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..Brunner Syndrome (C563156)
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..Bullous Dystrophy, Hereditary Macular Type (C563065)
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..CAHMR syndrome (C537959)
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..Camera Marugo Cohen syndrome (C537964)
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..Cantalamessa Baldini Ambrosi syndrome (C537981)
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..Cantu Sanchez-Corona Fragoso syndrome (C535571)
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..Cartwright Nelson Fryns syndrome (C535917)
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..Cataract, Congenital, with Mental Impairment and Dentate Gyrus Atrophy (C564353)
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..Cataracts, ataxia, short stature, and mental retardation (C535345)
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..Cataracts, Congenital, with Sensorineural Deafness, Down Syndrome-Like Facial Appearance, Short Stature, and Mental Retardation (C563390)
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..Cephalin Lipidosis (C565872)
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..Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2 (C567656)
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..Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 (C567690)
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..Cerebral Cavernous Malformations 2 (C566394)
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..Cerebral Cavernous Malformations 3 (C566393)
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..Cerebrocostomandibular Syndrome (C562538)
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..Cerebrofaciothoracic Dysplasia (C565862)
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..Cerebrooculofacioskeletal Syndrome 2 (C565185)
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..Cerebrooculofacioskeletal Syndrome 4 (C565184)
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..Cerebrooculonasal Syndrome (C565313)
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..Choroid plexus calcification with mental retardation (C535357)
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..CHROMOSOME 13q14 DELETION SYNDROME (OMIM:613884)
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..Chromosome 15q13.3 Microdeletion Syndrome (C567439)
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..Chromosome 15q26-Qter Deletion Syndrome (C567232)
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..CHROMOSOME 17p13.1 DELETION SYNDROME (OMIM:613776)
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..Chromosome 17q21.31 Deletion Syndrome (C566476)
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..Chromosome 18 Pericentric Inversion (C563734)
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..Chromosome 1q21.1 Duplication Syndrome (C567290)
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..Chromosome 1q43-Q44 Deletion Syndrome (C567346)
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..Chromosome 2q31.2 Deletion Syndrome (C567344)
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..Chromosome 2q32-Q33 Deletion Syndrome (C567350)
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..Chromosome 3q29 Deletion Syndrome (C567184)
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..CHROMOSOME 7q11.23 DELETION SYNDROME, DISTAL, 1.2-MB (OMIM:613729)
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..CHROMOSOME 8q21.11 DELETION SYNDROME (OMIM:614230)
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..Chromosome Xq28 Duplication Syndrome (C567580)
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..Chudley-Rozdilsky syndrome (C535458)
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..Cleft Palate, Isolated, And Mental Retardation (C566991)
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..Coffin syndrome 1 (C536435)
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..Coffin-Siris syndrome (C536436)
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..Cohen syndrome (C536438)
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..Coloboma, cleft lip/palate and mental retardation syndrome (C535971)
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..Coloboma, Uveal, with Cleft Lip and Palate and Mental Retardation (C565173)
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..Coloboma-Obesity-Hypogenitalism-Mental Retardation Syndrome (C566623)
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..Convulsive Disorder, Familial, with Prenatal or Early Onset (C565678)
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..Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia (C564509)
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..Cortical Blindness, Retardation, and Postaxial Polydactyly (C565674)
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..Craniofaciofrontodigital Syndrome (C567298)
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..Craniosynostosis Mental Retardation Clefting Syndrome (C565663)
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..Craniosynostosis-Mental Retardation Syndrome of Lin and Gettig (C565664)
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..Cree Mental Retardation Syndrome (C564654)
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..Cri-du-Chat Syndrome (D003410) 6
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..Cryohydrocytosis, Stomatin-Deficient, with Mental Retardation, Seizures, Cataracts, and Massive Hepatosplenomegaly (C563840)
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..Cubitus Valgus with Mental Retardation and Unusual Facies (C564510)
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..Curatolo Cilio Pessagno syndrome (C536701)
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..Cutis Verticis Gyrata and Mental Deficiency (C565661)
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..Cystic Fibrosis with Helicobacter Pylori Gastritis, Megaloblastic Anemia, and Subnormal Mentality (C565658)
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..Davis Lafer syndrome (C535989)
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..De Barsy syndrome (C535990)
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..De Lange Syndrome (D003635) 1
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..De Sanctis-Cacchione syndrome (C535992)
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..Deafness, Cochlear, with Myopia and Intellectual Impairment (C565645)
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..Deafness, congenital onychodystrophy, recessive form (C538204)
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..Devriendt syndrome (C535947)
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..Diabetes Insipidus, Nephrogenic, with Mental Retardation and Intracerebral Calcification (C565632)
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..Dicarboxylicaminoaciduria (C536171)
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..Digitorenocerebral Syndrome (C563052)
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..Dislocated Elbows, Bowed Tibias, Scoliosis, Deafness, Cataract, Microcephaly, And Mental Retardation (C566408)
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..Down Syndrome (D004314) 6
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..Dubowitz syndrome (C535718)
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..Duker Weiss Siber syndrome (C535719)
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..Duplication 15q11-q13 Syndrome (C557830)
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..Dwarfism, Low-Birth-Weight Type, with Unresponsiveness to Growth Hormone (C565615)
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..Dyggve-Melchior-Clausen syndrome (C535726)
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..Dysequilibrium syndrome (C535731)
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..Dysmyelination With Jaundice (C565610)
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..Ectodermal dysplasia mental retardation syndactyly (C538018)
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..Ectodermal Dysplasia, Hypohidrotic, with Hypothyroidism and Agenesis of the Corpus Callosum (C565605)
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..Elliott Ludman Teebi syndrome (C536204)
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..Emanuel syndrome (C535733)
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..Emphysema, Congenital, With Deafness, Penoscrotal Web, And Mental Retardation (C566519)
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..Encephalopathy with Intracranial Calcification, Growth Hormone Deficiency, Microcephaly, and Retinal Degeneration (C565594)
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..Epidermolysis bullosa, late-onset localized junctional, with mental retardation (C535492)
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..Epilepsy telangiectasia (C535497)
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..Epilepsy, Female-Restricted, with Mental Retardation (C564715)
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..Epilepsy, Photogenic, with Spastic Diplegia and Mental Retardation (C565587)
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..Facial Abnormalities, Kyphoscoliosis, and Mental Retardation (C565580)
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..Faciocardiomelic Syndrome (C567176)
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..Fallot complex with severe mental and growth retardation (C536608)
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..Feingold Trainer syndrome (C536179)
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..Fg Syndrome 5 (C564480)
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..Fibromatosis, Gingival, with Hypertrichosis and Mental Retardation (C565331)
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..Filippi syndrome (C538152)
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..Fine-Lubinsky syndrome (C537933)
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..Fitzsimmons Walson Mellor syndrome (C537937)
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..Fitzsimmons-McLachlan-Gilbert syndrome (C537058)
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..Fountain syndrome (C537270)
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..FRONTONASAL DYSPLASIA 3 (OMIM:613456)
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..Fryns-Aftimos Syndrome (C565258)
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..Garret Tripp syndrome (C535646)
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..Genitopatellar Syndrome (C565255)
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..Goniodysgenesis-Mental Retardation-Short Stature Syndrome (C564214)
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..Growth and Developmental Retardation, Ocular Ptosis, Cardiac Defect, and Anal Atresia (C565755)
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..Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate (C537405)
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..Growth Deficiency and Mental Retardation with Facial Dysmorphism (C565358)
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..Growth Failure, Microcephaly, Mental Retardation, Cataracts, Large Joint Contractures, Osteoporosis, Cortical Dysplasia, and Cerebellar Atrophy (C564264)
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..Growth mental deficiency syndrome of Myhre (C537620)
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..Gurrieri Sammito Bellussi syndrome (C537625)
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..Hair defect with photosensitivity and mental retardation (C537628)
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..Hall Riggs mental retardation syndrome (C535623)
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..Harrod Doman Keele syndrome (C535635)
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..Haspeslagh Fryns Muelenaere syndrome (C535844)
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..Histidinemia (C538320)
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..Hittner Hirsch Kreh syndrome (C538323)
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..Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate (C564484)
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..Hooft disease (C535329)
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..Hordnes Engebretsen Knudtson syndrome (C536067)
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..Hoyeraal Hreidarsson syndrome (C536068)
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..Hunter-McAlpine syndrome (C536072)
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..Hydronephrosis, Congenital, with Cleft Palate, Characteristic Facies, Hypotonia, and Mental Retardation (C565736)
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..Hydroxylysinuria (C565502)
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..Hyperleucine-Isoleucinemia (C562674)
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..Hyperlysinemia Due To Defect In Lysine Transport Into Mitochondria (C565499)
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..Hyperphosphatasia with Mental Retardation (C565495) 2
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..Hypertelorism, Severe, With Midface Prominence, Myopia, Mental Retardation, And Bone Fragility (C566988)
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..Hypertrichosis, hyperkeratosis, mental retardation, and distinctive facial features (C538391)
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..Hyperuricemia, Infantile, with Abnormal Behavior and Normal Hypoxanthine Guanine Phosphoribosyltransferase (C565489)
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..Hypogonadism with Low-Grade Mental Deficiency and Microcephaly (C565482)
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..Hypogonadism, Male, With Mental Retardation And Skeletal Anomalies (C564406)
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..Hypoparathyroidism-retardation-dysmorphism syndrome (C537157)
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..Hypospadias-Mental Retardation Syndrome (C563067)
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..Hypotonia-Cystinuria Syndrome (C564710)
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..Ichthyosis and male hypogonadism (C537365)
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..Ichthyosis, mental retardation, dwarfism, and renal impairment (C536274)
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..Ichthyosis-Mental Retardation Syndrome with Large Keratohyalin Granules in the Skin (C563402)
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..Indolylacroyl Glycinuria with Mental Retardation (C565466)
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..Iris Coloboma with Ptosis, Hypertelorism, and Mental Retardation (C565462)
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..Jagell Holmgren Hofer syndrome (C537364)
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..Johanson Blizzard syndrome (C535880)
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..Joubert Syndrome 7 (C566916)
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..Joubert Syndrome 9 (C567364)
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..Kahrizi Syndrome (C567196)
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..Kaler Garrity Stern syndrome (C537706)
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..Kapur Toriello syndrome (C537008)
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..Karandikar Maria Kamble syndrome (C537009)
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..Katsantoni Papadakou Lagoyanni syndrome (C537012)
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..Kaufman oculocerebrofacial syndrome (C537013)
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..KBG syndrome (C537015)
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..Kleefstra Syndrome (C563043)
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..Koone Rizzo Elias syndrome (C537023)
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..Kosztolanyi syndrome (C537024)
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..Kozlowski Ouvrier syndrome (C537508)
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..Kozlowski Rafinski Klicharska syndrome (C537509)
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..Kozlowski-Krajewska syndrome (C537615)
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..Kuzniecky syndrome (C538091)
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..Lambert syndrome (C538396)
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..Lenz Majewski hyperostotic dwarfism (C537115)
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..Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis (C565440)
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..Light Fixation Seizure Syndrome (C566367)
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..Limb Defects, Distal Transverse, with Mental Retardation and Spasticity (C565438)
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..Lipodystrophy, Generalized, with Mental Retardation, Deafness, Short Stature, and Slender Bones (C564283)
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..Lissencephaly 3 (C566908)
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..Lowry Maclean syndrome (C537037)
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..Lowry Wood syndrome (C537038)
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..Lubani Al Saleh Teebi syndrome (C537039)
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..Lynch Lee Murday syndrome (C537713)
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..Macrogyria, pseudobulbar palsy and mental retardation (C537722)
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..Macrosomia obesity macrocephaly ocular abnormalities (C535812)
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..Male pseudohermaphroditism/mental retardation syndrome, Verloes type (C535693)
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..Mandibulofacial Dysostosis with Mental Deficiency (C565420)
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..Marfanoid Mental Retardation Syndrome, Autosomal (C565410)
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..Marinesco-Sjogren-like syndrome (MSLS) (C535913)
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..Martin-Probst Deafness-Mental Retardation Syndrome (C564495)
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..Martsolf syndrome (C536028)
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..MASA (Mental Retardation, Aphasia, Shuffling Gait, Adducted Thumbs) Syndrome (C536029)
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..McDonough syndrome (C538158)
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..Mental and Growth Retardation with Amblyopia (C563591)
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..Mental Retardation associated with Psoriasis (C564107)
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..Mental retardation Mietens Weber type (C537444)
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..Mental retardation Smith Fineman Myers type (C537445)
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..Mental retardation spasticity ectrodactyly (C537446)
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..Mental retardation syndrome, Belgian type (C537447)
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..MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES (OMIM:613670)
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..Mental Retardation with Optic Atrophy, Facial Dysmorphism, Microcephaly, and Short Stature (C563810)
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..Mental Retardation with Spastic Paraplegia (C564099)
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..Mental retardation Wolff type (C537448)
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..MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS (OMIM:613671)
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..Mental Retardation, Autosomal Dominant 1 (C566947)
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..MENTAL RETARDATION, AUTOSOMAL DOMINANT 20 (OMIM:613443)
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..Mental Retardation, Autosomal Dominant 3 (C567241)
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..Mental Retardation, Autosomal Dominant 4 (C567240)
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..Mental Retardation, Autosomal Dominant 5 (C567234)
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..Mental Retardation, Autosomal Recessive 1 (C565406)
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..Mental Retardation, Autosomal Recessive 10 (C567013)
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..Mental Retardation, Autosomal Recessive 11 (C567012)
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..Mental Retardation, Autosomal Recessive 12 (C567019)
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..Mental Retardation, Autosomal Recessive 13 (C567714)
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..MENTAL RETARDATION, AUTOSOMAL RECESSIVE 16 (OMIM:614208)
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..Mental Retardation, Autosomal Recessive 2 (C564404)
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..Mental Retardation, Autosomal Recessive 3 (C563929)
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..Mental Retardation, Autosomal Recessive 4 (C567008)
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..Mental Retardation, Autosomal Recessive 5 (C567018)
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..Mental Retardation, Autosomal Recessive 6 (C567017)
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..Mental Retardation, Autosomal Recessive 7 (C567016)
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..Mental Retardation, Autosomal Recessive 8 (C567015)
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..Mental Retardation, Autosomal Recessive 9 (C567014)
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..Mental Retardation, Buenos Aires Type (C563095)
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..Mental Retardation, Fra12a Type (C566980)
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..Mental Retardation, Joint Hypermobility, And Skin Laxity, With Or Without Metabolic Abnormalities (C567209)
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..Mental retardation, keratoconus, febrile seizures, and sinoatrial block (C537452)
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..Mental retardation, macrocephaly, short stature and craniofacial dysmorphism (C537453)
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..Mental Retardation, Microcephaly, Epilepsy, And Coarse Face (C563342)
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..Mental Retardation, Microcephaly, Growth Retardation, Joint Contractures, and Facial Dysmorphism (C565246)
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..Mental Retardation, Severe, With Spasticity And Pigmentary Tapetoretinal Degeneration (C566429)
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..Mental Retardation, Short Stature, Facial Anomalies, and Joint Dislocations (C565248)
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..Mental Retardation, Skeletal Dysplasia, and Abducens Palsy (C564101)
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..Mental Retardation, X-Linked (D038901) 134
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..Mental Retardation, X-Linked, Syndromic 12 (C564106)
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..Mental Retardation, X-Linked, Syndromic, Christianson Type (C567484)
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..Mental Retardation, X-Linked, Syndromic, Turner Type (C567476)
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..Mental Retardation, X-Linked, Syndromic, Zdhhc9-Related (C567586)
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..Mental Retardation, X-Linked, With Panhypopituitarism (C567485)
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..Mental Retardation, X-Linked, Znf711-Related (C567583)
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..Metaphyseal Dysostosis, Mental Retardation, and Conductive Deafness (C565396)
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..Methionine Malabsorption Syndrome (C562682)
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..Microcephalic primordial dwarfism Toriello type (C537321)
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..Microcephaly cervical spine fusion anomalies (C537325)
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..Microcephaly deafness syndrome (C537326)
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..Microcephaly seizures mental retardation heart disorders (C537544)
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..Microcephaly sparse hair mental retardation seizures (C537545)
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..Microcephaly with Mental Retardation and Digital Anomalies (C567101)
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..Microcephaly, corpus callosum dysgenesis and cleft lip-palate (C537547)
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..Microcephaly, Facial Abnormalities, Micromelia, and Mental Retardation (C566361)
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..Microcephaly, Macrotia, And Mental Retardation (C566525)
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..Microphthalmia and mental deficiency (C537462)
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..Mirhosseini-Holmes-Walton syndrome (C538367)
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..Mohr-Tranebjaerg syndrome (C535808)
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..Mollica Pavone Antener syndrome (C535809)
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..MOMES Syndrome (C564660)
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..Morillo-Cucci Passarge syndrome (C536983)
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..MORM syndrome (C536984)
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..Mowat-Wilson syndrome (C536990)
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..Muscular Dystrophy, Congenital, associated with Calf Hypertrophy, Microcephaly, and Severe Mental Retardation (C565506)
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..Muscular Dystrophy, Congenital, plus Mental Retardation (C565505)
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..Muscular Dystrophy, Congenital, Type 1D (C563844)
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..MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 (OMIM:613155)
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..MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2 (OMIM:613156)
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..MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 (OMIM:613151)
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..MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 (OMIM:608840)
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..Myotonia with Skeletal Abnormalities and Mental Retardation (C564967)
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..N syndrome (C536108)
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..Nakamura Osame syndrome (C538335)
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..Neuhauser syndrome (C536143)
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..Neurofaciodigitorenal syndrome (C537388)
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..Neurologic Disease, Infantile Multisystem, with Osseous Fragility (C564954)
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..NF1 Microdeletion Syndrome (C563524)
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..NF1 Microduplication Syndrome (C567173)
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..Nicolaides Baraitser syndrome (C536116)
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..Oculodigitoesophagoduodenal syndrome (C537734)
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..Oliver Syndrome (C564931)
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..Oliver-McFarlane syndrome (C536554)
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..Onychotrichodysplasia and neutropenia (C537752)
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..Ophthalmoplegia, Progressive, with Scrotal Tongue and Mental Deficiency (C563498)
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..Opitz trigonocephaly syndrome (C537418)
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..Osteolysis syndrome recessive (C536052)
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..PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS (OMIM:600176)
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..Palant cleft palate syndrome (C538102)
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..Pallister W syndrome (C538106)
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..Parastremmatic dwarfism (C537172)
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..Parkinsonism, early onset with mental retardation (C537179)
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..Pashayan syndrome (C536303)
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..Patella hypoplasia mental retardation (C536308)
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..Pavone Fiumara Rizzo syndrome (C536313)
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..Perisylvian syndrome (C536658)
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..Perniola Krajewska Carnevale syndrome (C536660)
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..Pfeiffer Kapferer syndrome (C537887)
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..Pfeiffer Mayer syndrome (C537888)
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..Pfeiffer Tietze Welte syndrome (C537891)
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..Pilotto syndrome (C537400)
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..Pitt-Hopkins syndrome (C537403)
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..Piussan Lenaerts Mathieu syndrome (C537511)
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..Prader-Willi Syndrome (D011218) 2
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..Primrose syndrome (C536420)
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..Prolonged Bleeding Time, Brachydactyly, and Mental Retardation (C564207)
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..Proud Syndrome (C563110)
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..Prune Belly Syndrome with Pulmonic Stenosis, Mental Retardation, and Deafness (C562894)
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..Pseudoaminopterin syndrome (C535823)
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..Pseudouridinuria and Mental Defect (C564864)
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..Pterygium colli mental retardation digital anomalies (C535831)
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..Qazi Markouizos syndrome (C536259)
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..Radioulnar synostosis retinal pigment abnormalities (C536270)
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..Ramon Syndrome (C535285)
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..Ramos Arroyo Clark syndrome (C535286)
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..Reardon Wilson Cavanagh syndrome (C535295)
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..Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation (C567038)
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..Retinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism (C564841)
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..Richards-Rundle syndrome (C535674)
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..Robin Sequence with Distinctive Facial Appearance and Brachydactyly (C563880)
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..Rolandic Epilepsy, Mental Retardation, And Speech Dyspraxia, Autosomal Dominant (C563392)
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..Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked (C564467)
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..Rubinstein-Taybi Syndrome (D012415) 2
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..Rud Syndrome (C535878)
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..Ruzicka Goerz Anton syndrome (C537192)
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..Sammartino De Crecchio Syndrome (C537229)
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..Sao Paulo MCA/MR Syndrome (C563119)
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..Scaphocephaly, Maxillary Retrusion, And Mental Retardation (C566511)
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..SCARF syndrome (C536625)
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..Schinzel-Giedion syndrome (C536632)
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..Schofer Beetz Bohl syndrome (C535949)
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..Scholte syndrome (C536638)
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..Schrander-Stumpel Theunissen Hulsmans syndrome (C536639)
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..Sclerosing bone dysplasia mental retardation (C537523)
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..Scott Bryant Graham syndrome (C537528)
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..Seckel Syndrome 3 (C563881)
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..SECKEL SYNDROME 4 (OMIM:613676)
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..Seemanova Lesny syndrome (C537536)
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..SeSAME syndrome (C557674)
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..Short Stature, Mental Retardation, Callosal Agenesis, Heminasal Hypoplasia, Microphthalmia, And Atypical Clefting (C566989)
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..Simpson-Golabi-Behmel syndrome (C537340)
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..Singh Chhaparwal Dhanda syndrome (C537341)
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..Skeletal Defects, Genital Hypoplasia, And Mental Retardation (C567306)
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..Sketetal dysplasia coarse facies mental retardation (C536671)
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..Spastic Ataxia (C564815)
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..Spastic diplegia infantile type (C537481)
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..Spastic paraplegia 14, autosomal recessive (C537486)
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..Spastic Paraplegia 18, Autosomal Recessive (C567628)
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..Spastic Paraplegia 32, Autosomal Recessive (C566983)
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..Spastic paraplegia epilepsy mental retardation (C536869)
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..Spastic Paraplegia, Ataxia, And Mental Retardation (C564378)
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..Spastic Paraplegia, Sensorineural Deafness, Mental Retardation, And Progressive Nephropathy (C566682)
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..Spastic Paresis, Glaucoma, and Mental Retardation (C564809)
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..Spastic Quadriplegia, Retinitis Pigmentosa, and Mental Retardation (C564808)
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..Spinal Muscular Atrophy with Mental Retardation (C564807)
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..Spinal Muscular Atrophy with Microcephaly and Mental Subnormality (C564806)
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..Spondyloepimetaphyseal dysplasia, Genevieve type (C535785)
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..Spondyloepiphyseal Dysplasia Tarda with Mental Retardation (C564796)
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..Spondyloepiphyseal Dysplasia With Coronal Craniosynostosis, Cataracts, Cleft Palate, And Mental Retardation (C566515)
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..Stevenson-Carey Syndrome (C567446)
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..Sucrosuria, Hiatus Hernia and Mental Retardation (C564792)
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..SUPERNUMERARY DER(22)t(8 (OMIM:613700)
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..Tamari Goodman syndrome (C536896)
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..Temple-Baraitser Syndrome (C567516)
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..Temtamy preaxial brachydactyly syndrome (C536958)
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..Tetrasomy X (C536502)
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..Tonoki syndrome (C536967)
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..Trichodental syndrome (C536551)
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..TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH (OMIM:601675)
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..Tryptophanuria With Dwarfism (C562658)
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..Tsukahara Syndrome (C566376)
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..Ulna hypoplasia with mental retardation (C536934)
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..Ulnar Hypoplasia with Mental Retardation (C564757)
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..Upton Young syndrome (C536473)
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..Van Bogaert-Hozay syndrome (C536526)
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..Van Den Bosch Syndrome (C563129)
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..Van Maldergem Wetzburger Verloes syndrome (C536530)
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..Vasquez Hurst Sotos syndrome (C536533)
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..Verloes Gillerot Fryns syndrome (C536539)
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..Viljoen Kallis Voges syndrome (C536349)
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..Vitiligo, Progressive, with Mental Retardation and Urethral Duplication (C564739)
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..Volcke Soekarman syndrome (C537718)
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..WAGR Syndrome (D017624) 2
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..Walker Dyson syndrome (C536568)
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..Warburg Sjo Fledelius syndrome (C536681)
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..Warburton Anyane Yeboa syndrome (C536682)
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..Wiedemann Grosse Dibbern syndrome (C536704)
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..Wiedemann Oldigs Oppermann syndrome (C536705)
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..Williams Syndrome (D018980) 1
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..Winship Viljoen Leary syndrome (C536711)
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..Woodhouse Sakati syndrome (C536742)
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..Worster Drought syndrome (C536747)
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..Yorifuji Okuno syndrome (C536714)
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..Young Hughes syndrome (C536715)
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..Young Simpson syndrome (C536717)
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..Zazam Sheriff Phillips syndrome (C536723)
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..Zechi-Ceide Syndrome (C567865)
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..Zerres Rietschel Majewski syndrome (C536724)
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..Zlotogora-Ogur syndrome (C536726)
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..Zunich neuroectodermal syndrome (C536729)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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