oculocutaneous albinism type VII
oculocutaneous albinism that has material basis in an autosomal recessive mutation of C10orf11 on chromosome 10q22.2-q22.3
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oculocutaneous albinism type VII
Summary
oculocutaneous albinism type VII is a rare disease[1].
Key Facts
- oculocutaneous albinism type VII's instance of is recorded as rare disease[2].
- oculocutaneous albinism type VII's instance of is recorded as class of disease[3].
- oculocutaneous albinism type VII's subclass of is recorded as oculocutaneous albinism[4].
- oculocutaneous albinism type VII's OMIM ID is recorded as 615179[5].
- oculocutaneous albinism type VII's Disease Ontology ID is recorded as DOID:0070100[6].
- oculocutaneous albinism type VII's Orphanet ID is recorded as 352745[7].
- oculocutaneous albinism type VII's genetic association is recorded as LRMDA[8].
- oculocutaneous albinism type VII's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0070100[9].
- oculocutaneous albinism type VII's exact match is recorded as http://identifiers.org/doid/DOID:0070100[10].
- oculocutaneous albinism type VII's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_352745[11].
- oculocutaneous albinism type VII's UMLS CUI is recorded as C3808786[12].
- oculocutaneous albinism type VII's ICD-10-CM is recorded as E70.3[13].
- oculocutaneous albinism type VII's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- oculocutaneous albinism type VII's Mondo ID is recorded as MONDO_0014070[15].
- oculocutaneous albinism type VII's UniProt disease ID is recorded as DI-03749[16].