Disease Browser
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Parent Node: Fetal Growth Retardation (D005317) | Parent Node: Holoprosencephaly (D016142) | Parent Node: Microcephaly (D008831) | ..Starting node ..Lambotte syndrome (C537549)
| Child Nodes:
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Sister Nodes: | ..Absent Eyebrows and Eyelashes with Mental Retardation (C563111)
| ..Achalasia microcephaly (C536010)
| ..Agammaglobulinemia, microcephaly, and severe dermatitis (C538055)
| ..Alaninuria with Microcephaly, Dwarfism, Enamel Hypoplasia, and Diabetes Mellitus (C565968)
| ..Amish lethal microcephaly (C538247)
| ..Anonychia, Total, with Microcephaly (C564606)
| ..Aphalangia syndactyly microcephaly (C537787)
| ..Ataxia-Microcephaly-Cataract Syndrome (C563086)
| ..Autosomal Recessive Primary Microcephaly (C579935)
| ..Baetz-Greenwalt syndrome (C537795)
| ..BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA (OMIM:251290)
| ..Baraitser Brett Piesowicz syndrome (C537905)
| ..Battaglia Neri syndrome (C537662)
| ..BEAULIEU-BOYCOTT-INNES SYNDROME (OMIM:613680)
| ..Bixler Christian Gorlin syndrome (C537632)
| ..Boudhina Yedes Khiari syndrome (C537939)
| ..Brachydactyly, Type A2, With Microcephaly (C565894)
| ..Branchial arch syndrome X-linked (C537102)
| ..Bullous Dystrophy, Hereditary Macular Type (C563065)
| ..CAMFAK syndrome (C537965)
| ..Cardiac Malformation, Cleft Lip-Palate, Microcephaly and Digital Anomalies (C563414)
| ..Cataract, Microcephaly, Arthrogryposis, Kyphosis Syndrome (C566861)
| ..Chromosomal Instability with Tissue-Specific Radiosensitivity (C565848)
| ..Chromosome 15q26-Qter Deletion Syndrome (C567232)
| ..CHROMOSOME 17p13.1 DELETION SYNDROME (OMIM:613776)
| ..CHROMOSOME 3pter-p25 DELETION SYNDROME (OMIM:613792)
| ..CK SYNDROME (OMIM:300831)
| ..Cohen syndrome (C536438)
| ..Craniosynostosis Microcephaly with Chromosomal Breakage and Other Abnormalities (C565667)
| ..Dislocated Elbows, Bowed Tibias, Scoliosis, Deafness, Cataract, Microcephaly, And Mental Retardation (C566408)
| ..Dubowitz syndrome (C535718)
| ..Ellis Yale Winter syndrome (C536205)
| ..Encephalopathy with Intracranial Calcification, Growth Hormone Deficiency, Microcephaly, and Retinal Degeneration (C565594)
| ..Extrasystoles, Multiform Ventricular, with Short Stature, Hyperpigmentation and Microcephaly (C565032)
| ..Filippi syndrome (C538152)
| ..FORSYTHE-WAKELING SYNDROME (OMIM:613606)
| ..Galloway Mowat syndrome (C537548)
| ..GOMBO syndrome (C537284)
| ..Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate (C537405)
| ..Growth Deficiency and Mental Retardation with Facial Dysmorphism (C565358)
| ..Hadziselimovic Syndrome (C567850)
| ..Halal syndrome (C535622)
| ..Hersh Podruch Weisskopk syndrome (C538114)
| ..Hoyeraal Hreidarsson syndrome (C536068)
| ..Hypogonadism with Low-Grade Mental Deficiency and Microcephaly (C565482)
| ..Hypospadias-Mental Retardation Syndrome (C563067)
| ..Jejunal Atresia with Microcephaly and Ocular Anomalies (C565460)
| ..Jorgenson Lenz syndrome (C536292)
| ..Kaufman oculocerebrofacial syndrome (C537013)
| ..Lambotte syndrome (C537549)
| ..Lissencephaly 3 (C566908)
| ..Lowry Wood syndrome (C537038)
| ..Lymphedema, microcephaly and chorioretinopathy syndrome (C537711)
| ..MacDermot Winter syndrome (C537714)
| ..Marfanoid Habitus with Microcephaly and Glomerulonephritis (C565411)
| ..MEHMO syndrome (C537451)
| ..Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia (C567466)
| ..Mental Retardation, Microcephaly, Epilepsy, And Coarse Face (C563342)
| ..Mental Retardation, X-Linked, Syndromic 9 (C567474)
| ..Mental Retardation, X-Linked, Syndromic, Christianson Type (C567484)
| ..Microcephalic osteodysplastic primordial dwarfism, type 1 (C537577)
| ..Microcephalic osteodysplastic primordial dwarfism, type 3 (C537320)
| ..Microcephalic Osteodysplastic Primordial Dwarfism, Type II (C565898)
| ..Microcephalic primordial dwarfism Toriello type (C537321)
| ..Microcephaly albinism digital anomalies syndrome (C537322)
| ..Microcephaly autosomal dominant (C537323)
| ..Microcephaly cervical spine fusion anomalies (C537325)
| ..Microcephaly deafness syndrome (C537326)
| ..Microcephaly microphthalmos blindness (C537541)
| ..Microcephaly nonsyndromal (C537542)
| ..Microcephaly pontocerebellar hypoplasia dyskinesia (C537543)
| ..Microcephaly seizures genital hypoplasia (C537540)
| ..Microcephaly seizures mental retardation heart disorders (C537544)
| ..Microcephaly sparse hair mental retardation seizures (C537545)
| ..Microcephaly with Chemotactic Defect and Transient Hypogammaglobulinemia (C565381)
| ..Microcephaly with Chorioretinopathy, Autosomal Dominant (C563583)
| ..Microcephaly with Chorioretinopathy, Autosomal Recessive (C565379)
| ..Microcephaly with Mental Retardation and Digital Anomalies (C567101)
| ..Microcephaly with Simplified Gyral Pattern (C566332)
| ..Microcephaly with spastic quadriplegia (C537546)
| ..Microcephaly, Congenital Heart Disease, Unilateral Renal Agenesis, and Hyposegmented Lungs (C563341)
| ..Microcephaly, corpus callosum dysgenesis and cleft lip-palate (C537547)
| ..Microcephaly, Growth Retardation, Cataract, Hearing Loss, And Unusual Appearance (C567849)
| ..Microcephaly, Macrotia, And Mental Retardation (C566525)
| ..Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism (C537686)
| ..MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY (OMIM:613668)
| ..Microcephaly, Primary Autosomal Recessive, 1 (C565384)
| ..Microcephaly, Primary Autosomal Recessive, 2 (C565794)
| ..Microcephaly, Primary Autosomal Recessive, 3 (C565746)
| ..Microcephaly, Primary Autosomal Recessive, 4 (C565792)
| ..Microcephaly, Primary Autosomal Recessive, 5 (C563871)
| ..Microcephaly, Primary Autosomal Recessive, 5, with Simplified Gyral Pattern (C567221)
| ..Microcephaly, Primary Autosomal Recessive, 6 (C564247)
| ..Microcephaly, Primary Autosomal Recessive, 7 (C567198)
| ..Microcephaly, Retinitis Pigmentosa, and Sutural Cataract (C563296)
| ..MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY (OMIM:613402)
| ..Microcephaly, Severe, with Skeletal Anomalies including Posterior Rib-Gap Defects (C566377)
| ..Microcephaly-Micromelia Syndrome (C565382)
| ..Microhydranencephaly (C537555)
| ..Microphthalmia and mental deficiency (C537462)
| ..Milner Khallouf Gibson syndrome (C537473)
| ..Mirhosseini-Holmes-Walton syndrome (C538367)
| ..Mowat-Wilson syndrome (C536990)
| ..Muscular Dystrophy, Congenital, associated with Calf Hypertrophy, Microcephaly, and Severe Mental Retardation (C565506)
| ..Neu Laxova syndrome (C536405)
| ..Nijmegen Breakage Syndrome-Like Disorder (C567767)
| ..Oculodigitoesophagoduodenal syndrome (C537734)
| ..Oculopalatocerebral Syndrome (C564935)
| ..Osteogenesis imperfecta congenita, microcephaly, and cataracts (C537558)
| ..Paine syndrome (C538101)
| ..Partington Anderson syndrome (C536299)
| ..Phosphoglycerate Dehydrogenase Deficiency (C566618)
| ..Phosphoserine Aminotransferase Deficiency (C567032)
| ..PONTOCEREBELLAR HYPOPLASIA, TYPE 4 (OMIM:225753)
| ..Porencephaly (D065708) 1
| ..Raine syndrome (C535282)
| ..RAJAB SYNDROME (OMIM:613658)
| ..Sammartino De Crecchio Syndrome (C537229)
| ..Say Barber Miller syndrome (C536618)
| ..Say syndrome (C536621)
| ..Schimke X-linked mental retardation syndrome (C536630)
| ..Seckel syndrome 1 (C537533)
| ..Seckel syndrome 2 (C537534)
| ..Seckel Syndrome 3 (C563881)
| ..SECKEL SYNDROME 4 (OMIM:613676)
| ..Secretory Diarrhea, Myopathy, and Deafness (C564382)
| ..Seemanova Lesny syndrome (C537536)
| ..Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation (C566970)
| ..Silengo Lerone Pelizza syndrome (C537336)
| ..Spastic Paraplegia, Optic Atrophy, Microcephaly, And Xy Sex Reversal (C566409)
| ..Spinal Muscular Atrophy with Microcephaly and Mental Subnormality (C564806)
| ..Spondyloepimetaphyseal dysplasia, Genevieve type (C535785)
| ..Teebi Kaurah syndrome (C536948)
| ..Trichodental syndrome (C536551)
| ..Tsukahara Syndrome (C566376)
| ..Warburg Sjo Fledelius syndrome (C536681)
| ..Warburton Anyane Yeboa syndrome (C536682)
| ..Winship Viljoen Leary syndrome (C536711)
| ..Zerres Rietschel Majewski syndrome (C536724)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 6185 |
Name: | Lambotte syndrome |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D005317|MESH:D008831|MESH:D016142 |
TreeNumbers: | C05.660.207.410/C537549 |C05.660.207.620/C537549 |C10.500.034.875/C537549 |C10.500.507.400.500/C537549 |C13.703.277.370/C537549 |C16.131.077.410/C537549 |C16.131.260.380/C537549 |C16.131.621.207.410/C537549 |C16.131.621.207.620/C537549 |C16.131.666.034.875/C53754 |
Synonyms: | Microcephaly, holoprosencephaly, and intrauterine growth retardation |
Slim Mappings: | Congenital abnormality|Fetal disease|Genetic disease (inborn)|Musculoskeletal disease|Nervous system disease|Pathology (process)|Pregnancy complication |
Reference: |
MedGen: C537549
MeSH: C537549
OMIM: 245552;
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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