Usher syndrome type 1C
Usher syndrome type 1 that has material basis in homozygous or compound heterozygous mutation in the USH1C gene on chromosome 11p15
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Usher syndrome type 1C
Summary
Usher syndrome type 1C is a rare disease[1].
Key Facts
- Usher syndrome type 1C's instance of is recorded as rare disease[2].
- Usher syndrome type 1C's instance of is recorded as class of disease[3].
- Usher syndrome type 1C's subclass of is recorded as Usher syndrome type 1[4].
- Usher syndrome type 1C's OMIM ID is recorded as 276904[5].
- Usher syndrome type 1C's Disease Ontology ID is recorded as DOID:0110830[6].
- Usher syndrome type 1C's genetic association is recorded as USH1C[7].
- Usher syndrome type 1C's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110830[8].
- Usher syndrome type 1C's exact match is recorded as http://identifiers.org/doid/DOID:0110830[9].
- Usher syndrome type 1C's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_231169[10].
- Usher syndrome type 1C's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_886[11].
- Usher syndrome type 1C's UMLS CUI is recorded as C1848604[12].
- Usher syndrome type 1C's ICD-10-CM is recorded as H35.5[13].
- Usher syndrome type 1C's GARD rare disease ID is recorded as 5437[14].
- Usher syndrome type 1C's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- Usher syndrome type 1C's Mondo ID is recorded as MONDO_0010171[16].
- Usher syndrome type 1C's UniProt disease ID is recorded as DI-01113[17].