| Disease Browser
|
Parent Node:
 Alopecia (D000505) |
Parent Node:
Corneal Dystrophies, Hereditary (D003317) |
Parent Node:
Growth Disorders (D006130) |
..Starting node
.. Kuster Majewski Hammerstein syndrome (C538125)
|
Child Nodes:
|
Sister Nodes: |
..ACID-LABILE SUBUNIT DEFICIENCY (OMIM:615961)
|
..Acrocapitofemoral Dysplasia (C564334)
|
..Acrocephalopolydactylous Dysplasia (C573722)
|
..Acromegaloid features, overgrowth, cleft palate, and hernia (C535656)
|
..Agonadism, XY, with Mental Retardation, Short Stature, Retarded Bone Age, and Multiple Extragenital Malformations (C563429)
|
..Al Gazali Khidr Prem Chandran syndrome (C535616)
|
..Aphalangia syndactyly microcephaly (C537787)
|
..Auriculoosteodysplasia (C538271)
|
..Bellini Chiumello Rimoldi syndrome (C535652)
|
..Berk-Tabatznik syndrome (C535432)
|
..Bhaskar Jagannathan syndrome (C535437)
|
..Blepharophimosis with ptosis, syndactyly, and short stature (C536235)
|
..Borjeson-Forssman-Lehmann syndrome (C536575)
|
..Boudhina Yedes Khiari syndrome (C537939)
|
..BRACHYDACTYLY, TYPE E2 (OMIM:613382)
|
..Brooks-Wisniewski-Brown Syndrome (C563154)
|
..Cantalamessa Baldini Ambrosi syndrome (C537981)
|
..Cantu Sanchez-Corona Fragoso syndrome (C535571)
|
..Cataracts, ataxia, short stature, and mental retardation (C535345)
|
..Cataracts, Congenital, with Sensorineural Deafness, Down Syndrome-Like Facial Appearance, Short Stature, and Mental Retardation (C563390)
|
..Chitty Hall Baraitser syndrome (C535928)
|
..Chromosome 15q26-Qter Deletion Syndrome (C567232)
|
..Chromosome 18 Pericentric Inversion (C563734)
|
..CHROMOSOME 3pter-p25 DELETION SYNDROME (OMIM:613792)
|
..Clark-Baraitser syndrome (C536208)
|
..CODAS syndrome (C536434)
|
..Coffin syndrome 1 (C536435)
|
..Contractures ectodermal dysplasia cleft lip palate (C535465)
|
..Cote Katsantoni syndrome (C536449)
|
..COUSIN SYNDROME (OMIM:260660)
|
..Coxoauricular Syndrome (C565148)
|
..Craniofacial Abnormalities, Cataracts, Congenital Heart Disease, Sacral Neural Tube Defects, and Growth and Developmental Retardation (C564271)
|
..Creases, Infra-Auricular Cutaneous, with Tall Stature and Advanced Bone Age (C566543)
|
..Crumpled helices and small mouth (C536217)
|
..Curatolo Cilio Pessagno syndrome (C536701)
|
..Daish Hardman Lamont syndrome (C535770)
|
..Dermoids of cornea (C535376)
|
..DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FEATURES, AND SPARSE HAIR (OMIM:616901)
|
..Devriendt syndrome (C535947)
|
..Dubowitz syndrome (C535718)
|
..Dyschondrosteosis and Nephritis (C565080)
|
..ECTODERMAL DYSPLASIA/SHORT STATURE SYNDROME (OMIM:616029)
|
..Epithelial Squamous Dysplasia, Keratinizing Desquamative, of Urinary Tract (C565584)
|
..Extrasystoles, Multiform Ventricular, with Short Stature, Hyperpigmentation and Microcephaly (C565032)
|
..FACIAL DYSMORPHISM, IMMUNODEFICIENCY, LIVEDO, AND SHORT STATURE (OMIM:615139)
|
..Fallot complex with severe mental and growth retardation (C536608)
|
..Fetal Growth Retardation (D005317)  25  C:1
|
..Filippi syndrome (C538152)
|
..Floating-harbor syndrome (C537062)
|
..FORSYTHE-WAKELING SYNDROME (OMIM:613606)
|
..Frias syndrome (C535639)
|
..Game Friedman Paradice syndrome (C535406)
|
..Gay Feinmesser Cohen syndrome (C537676)
|
..GEMSS syndrome (C537679)
|
..GOMBO syndrome (C537284)
|
..Gomez Lopez Hernandez syndrome (C537285)
|
..Gonadal Dysgenesis, Hypergonadotropic, XX Type, Short Stature, and Recurrent Metabolic Acidosis (C565295)
|
..Goniodysgenesis-Mental Retardation-Short Stature Syndrome (C564214)
|
..Growth and Developmental Retardation, Ocular Ptosis, Cardiac Defect, and Anal Atresia (C565755)
|
..Growth Deficiency and Mental Retardation with Facial Dysmorphism (C565358)
|
..Growth Failure, Microcephaly, Mental Retardation, Cataracts, Large Joint Contractures, Osteoporosis, Cortical Dysplasia, and Cerebellar Atrophy (C564264)
|
..Growth mental deficiency syndrome of Myhre (C537620)
|
..GROWTH RESTRICTION, SEVERE, WITH DISTINCTIVE FACIES (OMIM:616489)
|
..Growth retardation, Alopecia, Pseudoanodontia and Optic atrophy (C535642)
|
..GROWTH RETARDATION, INTELLECTUAL DEVELOPMENTAL DISORDER, HYPOTONIA, AND HEPATOPATHY (OMIM:617093)
|
..Growth Retardation, Small and Puffy Hands and Feet, and Eczema (C565528)
|
..Hairy elbows (C535618)
|
..Heme Oxygenase 1 Deficiency (C564200)
|
..Hersh Podruch Weisskopk syndrome (C538114)
|
..Hooft disease (C535329)
|
..Hunter-McAlpine syndrome (C536072)
|
..Hutterite cerebroosteonephrodysplasia syndrome (C536074)
|
..Hypoparathyroidism-retardation-dysmorphism syndrome (C537157)
|
..Insulin-Like Growth Factor I Deficiency (C563867)
|
..Insulin-Like Growth Factor I, Resistance To (C564816)
|
..Insulin-Like Growth Factor I, Resistance to, due to Increased Binding Protein (C564817)
|
..Johanson Blizzard syndrome (C535880)
|
..Jorgenson Lenz syndrome (C536292)
|
..KOSAKI OVERGROWTH SYNDROME (OMIM:616592)
|
..Kozlowski Rafinski Klicharska syndrome (C537509)
|
..Krause-Kivlin syndrome (C537617)
|
..Kuster Majewski Hammerstein syndrome (C538125)
|
..Ladda Zonana Ramer syndrome (C538135)
|
..Langer mesomelic dysplasia (C537267)
|
..Laryngotracheal Stenosis, Progressive, with Short Stature and Arthropathy (C566379)
|
..Leri-Weil syndrome (C537119)
|
..Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis (C565440)
|
..LIG4 Syndrome (C564694)
|
..Lipodystrophy, Generalized, with Mental Retardation, Deafness, Short Stature, and Slender Bones (C564283)
|
..Lowry Maclean syndrome (C537037)
|
..Lowry Wood syndrome (C537038)
|
..MACROCEPHALY, MACROSOMIA, AND FACIAL DYSMORPHISM SYNDROME (OMIM:614192)
|
..Macrosomia Adiposa Congenita (C565425)
|
..Madelung Deformity (C562398)
|
..Malocclusion and Short Stature (C565421)
|
..Megarbane syndrome (C536145)
|
..Meier-Gorlin syndrome (C538012)
|
..Mental and Growth Retardation with Amblyopia (C563591)
|
..Mental retardation Mietens Weber type (C537444)
|
..Mental Retardation with Optic Atrophy, Facial Dysmorphism, Microcephaly, and Short Stature (C563810)
|
..Mental Retardation, Microcephaly, Growth Retardation, Joint Contractures, and Facial Dysmorphism (C565246)
|
..MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE (OMIM:300354)
|
..Mental Retardation, X-Linked, with Short Stature (C564527)
|
..Mental retardation-hypotonic facies syndrome, x-linked, 1 (C537457)
|
..Microcephaly cervical spine fusion anomalies (C537325)
|
..MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 1 (OMIM:616033)
|
..MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2 (OMIM:616817)
|
..MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH OR WITHOUT SEIZURES (OMIM:614833)
|
..Microdontia hypodontia short stature (C537553)
|
..Milner Khallouf Gibson syndrome (C537473)
|
..MIRAGE SYNDROME (OMIM:617053)
|
..Mitochondrial myopathy with lactic acidosis (C537476) L: 00408;
|
..Mollica Pavone Antener syndrome (C535809)
|
..Morillo-Cucci Passarge syndrome (C536983)
|
..MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS (OMIM:245600)
|
..Myelodysplasia, Immunodeficiency, Facial Dysmorphism, Short Stature, and Psychomotor Delay (C563345)
|
..Nathalie syndrome (C538342)
|
..Neurofaciodigitorenal syndrome (C537388)
|
..Nijmegen Breakage Syndrome-Like Disorder (C567767)
|
..OGDEN SYNDROME (OMIM:300855)
|
..Omodysplasia type 1 (C537746)
|
..Onat syndrome (C537749)
|
..Osteolysis syndrome recessive (C536052)
|
..Partington Anderson syndrome (C536299)
|
..Pectus Excavatum, Macrocephaly, Short Stature, Dysplastic Nails (C563941)
|
..Petty Laxova Wiedemann syndrome (C537886)
|
..Pfeiffer Kapferer syndrome (C537887)
|
..Pfeiffer Mayer syndrome (C537888)
|
..Pfeiffer Palm Teller syndrome (C537889)
|
..PHOSPHOSERINE PHOSPHATASE DEFICIENCY (OMIM:614023)
|
..Pili torti developmental delay neurological abnormalities (C537398)
|
..Pilotto syndrome (C537400)
|
..Polydysspondyly (C565150)
|
..Premature aging, Okamoto type (C535270)
|
..Progeria short stature pigmented nevi (C536422)
|
..Progeroid Syndrome, Congenital, Petty Type (C567360)
|
..Qazi Markouizos syndrome (C536259)
|
..Radioulnar synostosis retinal pigment abnormalities (C536270)
|
..RAJAB SYNDROME (OMIM:613658)
|
..Ramon Syndrome (C535285)
|
..Reardon Wilson Cavanagh syndrome (C535295)
|
..Renal Tubular Acidosis, Distal, With Nephrocalcinosis, Short Stature, Mental Retardation, And Distinctive Facies (C566918)
|
..RETINAL DYSTROPHY, JUVENILE CATARACTS, AND SHORT STATURE SYNDROME (OMIM:616108)
|
..Rhizomelic dysplasia, scoliosis, and retinitis pigmentosa (C537610)
|
..Rodrigues blindness (C535865)
|
..Rommen Mueller Sybert syndrome (C535871)
|
..Rowley-Rosenberg syndrome (C535874)
|
..Say Meyer syndrome (C536620)
|
..Say syndrome (C536621)
|
..Schaap Taylor Baraitser syndrome (C536626)
|
..Schimke X-linked mental retardation syndrome (C536630)
|
..Seemanova Lesny syndrome (C537536)
|
..Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation (C566970)
|
..SHORT STATURE AND ADVANCED BONE AGE, WITH OR WITHOUT EARLY-ONSET OSTEOARTHRITIS AND/OR OSTEOCHONDRITIS DISSECANS (OMIM:165800)
|
..Short stature syndrome, Brussels type (C537121)
|
..Short Stature, Facial Dysmorphism, Severe Brachydactyly, and Syndactyly (C567093)
|
..Short Stature, Idiopathic, X-Linked (C564479)
|
..SHORT syndrome (C537327)
|
..Slavotinek Pike Mills Hurst syndrome (C536672)
|
..Sonoda syndrome (C536680)
|
..Spastic paraplegia 9, autosomal dominant (C536868)
|
..Spondyloepimetaphyseal Dysplasia, Pakistani Type (C567551)
|
..Spondylometaphyseal dysplasia, 'corner fracture' type (C535793)
|
..Stern Lubinsky Durrie syndrome (C537488)
|
..Synostosis of Talus and Calcaneus with Short Stature (C566089)
|
..TATTON-BROWN-RAHMAN SYNDROME (OMIM:615879)
|
..TENORIO SYNDROME (OMIM:616260)
|
..THAUVIN-ROBINET-FAIVRE SYNDROME (OMIM:617107)
|
..Theodor Hertz Goodman syndrome (C536509)
|
..Thrombocytopenia Robin sequence (C536898)
|
..Thumb Agenesis, Short Stature, And Immunodeficiency (C564770)
|
..Thumb, Hypoplastic, with Choroid Coloboma, Poorly Developed Antihelix, and Deafness (C564769)
|
..Tonoki syndrome (C536967)
|
..Tsukahara Syndrome (C566376)
|
..Vater-Like Defects with Pulmonary Hypertension, Laryngeal Webs, and Growth Deficiency (C564244)
|
..VERHEIJ SYNDROME (OMIM:615583)
|
..Vertebral body fusion overgrowth (C536543)
|
..Viljoen Kallis Voges syndrome (C536349)
|
..Volcke Soekarman syndrome (C537718)
|
..Wellesley Carmen French syndrome (C536691)
|
..Wiedemann Grosse Dibbern syndrome (C536704)
|
..Winchester syndrome (C536709)
|
..Wittwer syndrome (C536737)
|
..Young Hughes syndrome (C536715)
|
..Zerres Rietschel Majewski syndrome (C536724)
|
..Zinc Deficiency, Neonatal, due to Low Breast Milk Zinc (C564286)
|
Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
|
