Leber congenital amaurosis 3
Leber congenital amaurosis that has material basis in mutation in the SPATA7 gene on chromosome 14q31
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Summary
Leber congenital amaurosis 3 is a rare disease[1].
Key Facts
- Leber congenital amaurosis 3's instance of is recorded as rare disease[2].
- Leber congenital amaurosis 3's instance of is recorded as class of disease[3].
- Leber congenital amaurosis 3's subclass of is recorded as Leber congenital amaurosis[4].
- Leber congenital amaurosis 3's subclass of is recorded as genetic disease[5].
- Leber congenital amaurosis 3's MeSH descriptor ID is recorded as C565814[6].
- Leber congenital amaurosis 3's OMIM ID is recorded as 604232[7].
- Leber congenital amaurosis 3's Disease Ontology ID is recorded as DOID:0110331[8].
- Leber congenital amaurosis 3's genetic association is recorded as SPATA7[9].
- Leber congenital amaurosis 3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110331[10].
- Leber congenital amaurosis 3's exact match is recorded as http://identifiers.org/doid/DOID:0110331[11].
- Leber congenital amaurosis 3's UMLS CUI is recorded as C1858677[12].
- Leber congenital amaurosis 3's UMLS CUI is recorded as C2751780[13].
- Leber congenital amaurosis 3's ICD-10-CM is recorded as H35.5[14].
- Leber congenital amaurosis 3's GARD rare disease ID is recorded as 9661[15].
- Leber congenital amaurosis 3's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- Leber congenital amaurosis 3's Mondo ID is recorded as MONDO_0011415[17].
- Leber congenital amaurosis 3's UniProt disease ID is recorded as DI-00631[18].