Leber congenital amaurosis 4

Summary

Leber congenital amaurosis 4 is a rare disease^[1].

Key Facts

• Leber congenital amaurosis 4's instance of is recorded as rare disease^[2].
• Leber congenital amaurosis 4's instance of is recorded as class of disease^[3].
• Leber congenital amaurosis 4's subclass of is recorded as Leber congenital amaurosis^[4].
• Leber congenital amaurosis 4's subclass of is recorded as genetic disease^[5].
• Leber congenital amaurosis 4's subclass of is recorded as autosomal recessive disease^[6].
• Leber congenital amaurosis 4's MeSH descriptor ID is recorded as C565778^[7].
• Leber congenital amaurosis 4's OMIM ID is recorded as 604393^[8].
• Leber congenital amaurosis 4's Disease Ontology ID is recorded as DOID:0110332^[9].
• Leber congenital amaurosis 4's genetic association is recorded as AIPL1^[10].
• Leber congenital amaurosis 4's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110332^[11].
• Leber congenital amaurosis 4's exact match is recorded as http://identifiers.org/doid/DOID:0110332^[12].
• Leber congenital amaurosis 4's UMLS CUI is recorded as C1858386^[13].
• Leber congenital amaurosis 4's UMLS CUI is recorded as C2751763^[14].
• Leber congenital amaurosis 4's UMLS CUI is recorded as C2751764^[15].
• Leber congenital amaurosis 4's ICD-10-CM is recorded as H35.5^[16].
• Leber congenital amaurosis 4's GARD rare disease ID is recorded as 9662^[17].
• Leber congenital amaurosis 4's on focus list of Wikimedia project is recorded as WikiProject Medicine^[18].
• Leber congenital amaurosis 4's Mondo ID is recorded as MONDO_0011458^[19].
• Leber congenital amaurosis 4's UniProt disease ID is recorded as DI-00632^[20].