Usher syndrome type 1F
Usher syndrome type 1 that has material basis in caused by homozygous or compound heterozygous mutation in the PCDH15 gene on chromosome 10q
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Usher syndrome type 1F
Summary
Usher syndrome type 1F is a rare disease[1].
Key Facts
- Usher syndrome type 1F's instance of is recorded as rare disease[2].
- Usher syndrome type 1F's instance of is recorded as class of disease[3].
- Usher syndrome type 1F's subclass of is recorded as Usher syndrome type 1[4].
- Usher syndrome type 1F's OMIM ID is recorded as 602083[5].
- Usher syndrome type 1F's OMIM ID is recorded as 602083[6].
- Usher syndrome type 1F's Disease Ontology ID is recorded as DOID:0110832[7].
- Usher syndrome type 1F's genetic association is recorded as PCDH15[8].
- Usher syndrome type 1F's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110832[9].
- Usher syndrome type 1F's exact match is recorded as http://identifiers.org/doid/DOID:0110832[10].
- Usher syndrome type 1F's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_231169[11].
- Usher syndrome type 1F's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_886[12].
- Usher syndrome type 1F's UMLS CUI is recorded as C1865885[13].
- Usher syndrome type 1F's ICD-10-CM is recorded as H35.5[14].
- Usher syndrome type 1F's GARD rare disease ID is recorded as 10043[15].
- Usher syndrome type 1F's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- Usher syndrome type 1F's Mondo ID is recorded as MONDO_0011186[17].
- Usher syndrome type 1F's UniProt disease ID is recorded as DI-01116[18].