Disease Browser
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Parent Node: Waardenburg Syndrome (D014849) | ..Starting node ..Waardenburg Syndrome, Type 2C (C564684)
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Sister Nodes: | ..ABCD syndrome (C535334)
| ..Anophthalmos with limb anomalies (C537769)
| ..Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease (C563789)
| ..Van der Hoeve Halbertsma Waardenburg Gualdi Syndrome (C538657)
| ..Waardenburg syndrome type 2 (C536463)
| ..Waardenburg syndrome type 2A (C536464)
| ..Waardenburg syndrome type 2B (C536465)
| ..Waardenburg Syndrome, Type 2C (C564684)
| ..Waardenburg Syndrome, Type 2D (C563839)
| ..Waardenburg syndrome, type 4 (C536467) 1
| ..Waardenburg Syndrome, Type 4b (C567680)
| ..Waardenburg Syndrome, Type 4c (C567679)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 11684 |
Name: | Waardenburg Syndrome, Type 2C |
Definition: | |
Alternative IDs: | OMIM:606662 |
ParentIDs: | MESH:D014849 |
TreeNumbers: | C16.131.077.938/C564684 |
Synonyms: | Waardenburg Syndrome, Type IIC |WS2C |
Slim Mappings: | Congenital abnormality |
Reference: |
MedGen: C564684
MeSH: C564684
OMIM: 606662;
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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