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Usher syndrome type 1F

http://purl.obolibrary.org/obo/DOID_0110832

An Usher syndrome type 1 that has_material_basis_in caused by homozygous or compound heterozygous mutation in the PCDH15 gene on chromosome 10q. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

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Term info

Label

Usher syndrome type 1F

Synonyms

USH1F
Usher syndrome type IF

database cross reference

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disease_ontology

DOID:0110832

Term relations

Subclass of:

Usher syndrome type 1
has material basis in some autosomal recessive inheritance