Usher syndrome type 1J
Usher syndrome type 1 that has material basis in caused by homozygous mutation in the CIB2 gene on chromosome 15q24
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Usher syndrome type 1J
Summary
Usher syndrome type 1J is a rare disease[1].
Key Facts
- Usher syndrome type 1J's instance of is recorded as rare disease[2].
- Usher syndrome type 1J's instance of is recorded as class of disease[3].
- Usher syndrome type 1J's subclass of is recorded as Usher syndrome type 1[4].
- Usher syndrome type 1J's OMIM ID is recorded as 614869[5].
- Usher syndrome type 1J's OMIM ID is recorded as 614869[6].
- Usher syndrome type 1J's Disease Ontology ID is recorded as DOID:0110836[7].
- Usher syndrome type 1J's genetic association is recorded as CIB2[8].
- Usher syndrome type 1J's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110836[9].
- Usher syndrome type 1J's exact match is recorded as http://identifiers.org/doid/DOID:0110836[10].
- Usher syndrome type 1J's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_231169[11].
- Usher syndrome type 1J's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_886[12].
- Usher syndrome type 1J's UMLS CUI is recorded as C3553944[13].
- Usher syndrome type 1J's ICD-10-CM is recorded as H35.5[14].
- Usher syndrome type 1J's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- Usher syndrome type 1J's Mondo ID is recorded as MONDO_0013935[16].
- Usher syndrome type 1J's UniProt disease ID is recorded as DI-03552[17].