Any Leber congenital amaurosis in which the cause of the disease is a mutation in the CRB1 gene. [ MONDO:patterns/disease_series_by_gene ]

This is just here as a test because I lose it

Term information

database cross reference
Subsets

gard_rare

abbreviation
LCA8 [ MONDO:Lexical https://omim.org/entry/613835 DOID:0110079 ]

conformsTo

http://purl.obolibrary.org/obo/mondo/patterns/specific_disease_by_dysfunctional_structure.yaml

definition

Any Leber congenital amaurosis in which the cause of the disease is a mutation in the CRB1 gene.

exactMatch

http://linkedlifedata.com/resource/umls/id/C3151202

http://purl.obolibrary.org/obo/DOID_0110079

http://identifiers.org/omim/613835

has exact synonym

Leber congenital amaurosis caused by mutation in CRB1

Leber congenital amaurosis 8

LCA8

CRB1 Leber congenital amaurosis

Leber congenital amaurosis type 8

id

MONDO:0013453

seeAlso

https://rarediseases.info.nih.gov/diseases/10881/leber-congenital-amaurosis-8