Disease Browser
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Parent Node: Abnormalities, Multiple (D000015) | Parent Node: Cleft Lip (D002971) | Parent Node: Cleft Palate (D002972) | Parent Node: Coloboma (D003103) | Parent Node: Ectromelia (D004480) | Parent Node: Hydrocephalus (D006849) | ..Starting node ..Yim Ebbin syndrome (C536713)
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Sister Nodes: | ..Aase Smith syndrome (C535332)
| ..Axenfeld-Rieger Anomaly with Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, and Skeletal Abnormalities (C566234)
| ..Baker Vinters syndrome (C537899)
| ..Beemer Ertbruggen syndrome (C537668)
| ..Bor-Duane hydrocephalus contiguous gene syndrome (C536574)
| ..Clark-Baraitser syndrome (C536208)
| ..Cole Carpenter syndrome (C535963)
| ..Cystic Kidney Disease with Ventriculomegaly (C565657)
| ..Daentl Towsend Siegel syndrome (C535768)
| ..Daish Hardman Lamont syndrome (C535770)
| ..Dandy-Walker Syndrome (D003616) 13
| ..Edinburgh Malformation Syndrome (C563051)
| ..Enamel Hypoplasia, Cataracts, and Aqueductal Stenosis (C563430)
| ..Game Friedman Paradice syndrome (C535406)
| ..Hydrocephalus With Cerebellar Agenesis (C564407)
| ..Hydrocephalus, Autosomal Dominant (C563973)
| ..Hydrocephalus, endocardial fibroelastosis, and cataracts (C535855)
| ..Hydrocephalus, Normal Pressure (D006850) 1
| ..Hydrocephalus, Skeletal Anomalies, and Mental Disturbance (C563413)
| ..Hydrocephalus, X-linked (C536078)
| ..Hydrocephalus, X-Linked, with Congenital Idiopathic Intestinal Pseudoobstruction (C564408)
| ..Hydrolethalus syndrome (C536079)
| ..Hydrolethalus Syndrome 1 (C565504)
| ..Iris dysplasia hypertelorism deafness (C535537)
| ..Kozlowski Brown Hardwick syndrome (C537506)
| ..Megalanecephaly Polymicrogyria-Polydactyly Hydrocephalus Syndrome (C566381)
| ..Osteochondrodysplasia, Rhizomelic, with Callosal Agenesis, Thrombocytopenia, Hydrocephalus, and Hypertension (C563478)
| ..Palmer Pagon syndrome (C538107)
| ..Radius absent anogenital anomalies (C535281)
| ..Schwartz Cohen-Addad Lambert syndrome (C535835)
| ..Thoracic Dysplasia-Hydrocephalus Syndrome (C564774)
| ..VACTERL Association With Hydrocephalus (C564751)
| ..VACTERL association with hydrocephaly, X-linked (C536520)
| ..VACTERL hydrocephaly (C536521)
| ..Vater Association With Hydrocephalus (C564752)
| ..Ventriculomegaly With Defects Of The Radius And Kidney (C566565)
| ..Waaler Aarskog syndrome (C536461)
| ..Yim Ebbin syndrome (C536713)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 11856 |
Name: | Yim Ebbin syndrome |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D000015|MESH:D002971|MESH:D002972|MESH:D003103|MESH:D004480|MESH:D006849 |
TreeNumbers: | C05.500.460.185/C536713 |C05.660.207.540.460.185/C536713 |C05.660.585.350/C536713 |C07.320.440.185/C536713 |C07.465.409.225/C536713 |C07.465.525.164/C536713 |C07.465.525.185/C536713 |C07.650.500.460.185/C536713 |C07.650.525.164/C536713 |C07.650.525.185/C536713 |C1 |
Synonyms: | Amelia, cleft lip, palate, hydrocephalus, iris coloboma |Brachial amelia, forebrain defects and facial clefts |Brachial Amelia, Forebrain Defects, and Facial Clefts |
Slim Mappings: | Congenital abnormality|Eye disease|Mouth disease|Musculoskeletal disease|Nervous system disease |
Reference: |
MedGen: C536713
MeSH: C536713
OMIM:
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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