Online Mendelian Inheritance in Man

Last uploaded: January 31, 2024
Preferred Name

WILDERVANCK SYNDROME

Synonyms

CERVICOOCULOACOUSTIC SYNDROME

ID

http://purl.bioontology.org/ontology/OMIM/314600

altLabel

CERVICOOCULOACOUSTIC SYNDROME

cui

C0265239

Has manifestation

http://purl.bioontology.org/ontology/OMIM/MTHU006801

http://purl.bioontology.org/ontology/OMIM/MTHU006799

http://purl.bioontology.org/ontology/OMIM/MTHU000574

http://purl.bioontology.org/ontology/OMIM/MTHU006802

http://purl.bioontology.org/ontology/OMIM/MTHU001183

http://purl.bioontology.org/ontology/OMIM/MTHU006803

http://purl.bioontology.org/ontology/OMIM/MTHU006800

http://purl.bioontology.org/ontology/OMIM/MTHU006798

MIMTYPEMEANING

Mendelian phenotype or locus, molecular basis unknown.

notation

314600

OMIM Entry Type

5

OMIM MimType Value

perc

prefLabel

WILDERVANCK SYNDROME

Scope Statement

Most patients are female [MISCELLANEOUS]

tui

T047

Delete Subject Author Type Created
No notes to display