Disease Browser
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Parent Node: Dandy-Walker Syndrome (D003616) | ..Starting node ..Dandy Walker cyst (C538507)
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Sister Nodes: | ..3C syndrome (C535313)
| ..Chitayat Moore Del Bigio syndrome (C535927)
| ..Craniosynostosis, sagittal, with Dandy-Walker malformation and hydrocephalus (C536790)
| ..Dandy Walker cyst (C538507)
| ..Dandy Walker malformation postaxial polydactyly (C535771)
| ..Dandy Walker variant (C535772)
| ..Dandy-walker malformation with mental retardation, macrocephaly, myopia, and brachytelephalangy (C535985)
| ..Dandy-Walker Malformation With Occipital Cephalocele, Autosomal Dominant (C567185)
| ..Mental retardation, X-linked, syndromic 5 (C535773)
| ..Nasopharyngeal teratoma with Dandy Walker diaphragmatic hernia (C538340)
| ..Renal hepatic pancreatic dysplasia Dandy Walker cyst (C537756)
| ..RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 (OMIM:208540)
| ..Volcke Soekarman syndrome (C537718)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 2964 |
Name: | Dandy Walker cyst |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D003616 |
TreeNumbers: | C10.228.140.252.300/C538507 |C10.228.140.602.288/C538507 |C10.228.140.631.450.500/C538507 |C10.500.205/C538507 |C16.131.666.205/C538507 |
Synonyms: | |
Slim Mappings: | Congenital abnormality|Nervous system disease |
Reference: |
MedGen: C538507
MeSH: C538507
OMIM:
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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