Leber congenital amaurosis 7
Leber congenital amaurosis that has material basis in mutation in the CRX gene on chromosome 19q13
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Leber congenital amaurosis 7
Summary
Leber congenital amaurosis 7 is a rare disease[1].
Key Facts
- Leber congenital amaurosis 7's instance of is recorded as rare disease[2].
- Leber congenital amaurosis 7's instance of is recorded as class of disease[3].
- Leber congenital amaurosis 7's subclass of is recorded as Leber congenital amaurosis[4].
- Leber congenital amaurosis 7's subclass of is recorded as genetic disease[5].
- Leber congenital amaurosis 7's subclass of is recorded as monogenic disease[6].
- Leber congenital amaurosis 7's OMIM ID is recorded as 613829[7].
- Leber congenital amaurosis 7's Disease Ontology ID is recorded as DOID:0110333[8].
- Leber congenital amaurosis 7's genetic association is recorded as CRX[9].
- Leber congenital amaurosis 7's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110333[10].
- Leber congenital amaurosis 7's exact match is recorded as http://identifiers.org/doid/DOID:0110333[11].
- Leber congenital amaurosis 7's UMLS CUI is recorded as C3151192[12].
- Leber congenital amaurosis 7's ICD-10-CM is recorded as H35.5[13].
- Leber congenital amaurosis 7's GARD rare disease ID is recorded as 10880[14].
- Leber congenital amaurosis 7's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- Leber congenital amaurosis 7's Mondo ID is recorded as MONDO_0013449[16].
- Leber congenital amaurosis 7's UniProt disease ID is recorded as DI-00635[17].