Usher syndrome type 1G
Usher syndrome type 1 that has material basis in caused by homozygous or compound heterozygous mutation in the USH1G gene on chromosome 17q25
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Usher syndrome type 1G
Summary
Usher syndrome type 1G is a rare disease[1].
Key Facts
- Usher syndrome type 1G's instance of is recorded as rare disease[2].
- Usher syndrome type 1G's instance of is recorded as class of disease[3].
- Usher syndrome type 1G's subclass of is recorded as Usher syndrome type 1[4].
- Usher syndrome type 1G's MeSH descriptor ID is recorded as C564643[5].
- Usher syndrome type 1G's OMIM ID is recorded as 606943[6].
- Usher syndrome type 1G's OMIM ID is recorded as 606943[7].
- Usher syndrome type 1G's Disease Ontology ID is recorded as DOID:0110834[8].
- Usher syndrome type 1G's genetic association is recorded as USH1G[9].
- Usher syndrome type 1G's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110834[10].
- Usher syndrome type 1G's exact match is recorded as http://identifiers.org/doid/DOID:0110834[11].
- Usher syndrome type 1G's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_231169[12].
- Usher syndrome type 1G's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_886[13].
- Usher syndrome type 1G's UMLS CUI is recorded as C1847089[14].
- Usher syndrome type 1G's ICD-10-CM is recorded as H35.5[15].
- Usher syndrome type 1G's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- Usher syndrome type 1G's Mondo ID is recorded as MONDO_0011748[17].
- Usher syndrome type 1G's UniProt disease ID is recorded as DI-01117[18].