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Usher syndrome type 1G

http://purl.obolibrary.org/obo/DOID_0110834

An Usher syndrome type 1 that has_material_basis_in caused by homozygous or compound heterozygous mutation in the USH1G gene on chromosome 17q25. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

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Term info

Label

Usher syndrome type 1G

Synonyms

USH1G
Usher syndrome type IG

database cross reference

has obo namespace

disease_ontology

DOID:0110834

Term relations

Subclass of:

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