| Disease Browser
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Parent Node:
 Abnormalities, Multiple (D000015) |
Parent Node:
Hydrocephalus (D006849) |
..Starting node
.. Kozlowski Brown Hardwick syndrome (C537506)
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Child Nodes:
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Sister Nodes: |
..Aase Smith syndrome (C535332)
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..Axenfeld-Rieger Anomaly with Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, and Skeletal Abnormalities (C566234)
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..Baker Vinters syndrome (C537899)
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..Beemer Ertbruggen syndrome (C537668)
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..Bor-Duane hydrocephalus contiguous gene syndrome (C536574)
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..Clark-Baraitser syndrome (C536208)
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..Cole Carpenter syndrome (C535963)
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..Cystic Kidney Disease with Ventriculomegaly (C565657)
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..Daentl Towsend Siegel syndrome (C535768)
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..Daish Hardman Lamont syndrome (C535770)
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..Dandy-Walker Syndrome (D003616)  13
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..Edinburgh Malformation Syndrome (C563051)
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..Enamel Hypoplasia, Cataracts, and Aqueductal Stenosis (C563430)
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..Game Friedman Paradice syndrome (C535406)
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..Hydrocephalus With Cerebellar Agenesis (C564407)
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..Hydrocephalus, Autosomal Dominant (C563973)
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..Hydrocephalus, endocardial fibroelastosis, and cataracts (C535855)
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..Hydrocephalus, Normal Pressure (D006850) 1
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..Hydrocephalus, Skeletal Anomalies, and Mental Disturbance (C563413)
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..Hydrocephalus, X-linked (C536078)
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..Hydrocephalus, X-Linked, with Congenital Idiopathic Intestinal Pseudoobstruction (C564408)
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..Hydrolethalus syndrome (C536079)
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..Hydrolethalus Syndrome 1 (C565504)
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..Iris dysplasia hypertelorism deafness (C535537)
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..Kozlowski Brown Hardwick syndrome (C537506)
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..Megalanecephaly Polymicrogyria-Polydactyly Hydrocephalus Syndrome (C566381)
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..Osteochondrodysplasia, Rhizomelic, with Callosal Agenesis, Thrombocytopenia, Hydrocephalus, and Hypertension (C563478)
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..Palmer Pagon syndrome (C538107)
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..Radius absent anogenital anomalies (C535281)
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..Schwartz Cohen-Addad Lambert syndrome (C535835)
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..Thoracic Dysplasia-Hydrocephalus Syndrome (C564774)
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..VACTERL Association With Hydrocephalus (C564751)
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..VACTERL association with hydrocephaly, X-linked (C536520)
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..VACTERL hydrocephaly (C536521)
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..Vater Association With Hydrocephalus (C564752)
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..Ventriculomegaly With Defects Of The Radius And Kidney (C566565)
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..Waaler Aarskog syndrome (C536461)
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..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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