Leber congenital amaurosis 17
Leber congenital amaurosis that has material basis in mutation in the GDF6 gene on chromosome 8q22
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Leber congenital amaurosis 17
Summary
Leber congenital amaurosis 17 is a rare disease[1].
Key Facts
- Leber congenital amaurosis 17's instance of is recorded as rare disease[2].
- Leber congenital amaurosis 17's instance of is recorded as class of disease[3].
- Leber congenital amaurosis 17's subclass of is recorded as Leber congenital amaurosis[4].
- Leber congenital amaurosis 17's subclass of is recorded as genetic disease[5].
- Leber congenital amaurosis 17's OMIM ID is recorded as 615360[6].
- Leber congenital amaurosis 17's Disease Ontology ID is recorded as DOID:0110217[7].
- Leber congenital amaurosis 17's genetic association is recorded as GDF6[8].
- Leber congenital amaurosis 17's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110217[9].
- Leber congenital amaurosis 17's exact match is recorded as http://identifiers.org/doid/DOID:0110217[10].
- Leber congenital amaurosis 17's UMLS CUI is recorded as C3715164[11].
- Leber congenital amaurosis 17's ICD-10-CM is recorded as H35.5[12].
- Leber congenital amaurosis 17's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- Leber congenital amaurosis 17's Mondo ID is recorded as MONDO_0014145[14].
- Leber congenital amaurosis 17's UniProt disease ID is recorded as DI-03831[15].