congenital stationary night blindness 1F
congenital stationary night blindness characterized by autosomal recessive inheritance that has material basis in compound heterozygous mutation in the LRIT3 gene on chromosome 4q25
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Summary
congenital stationary night blindness 1F is a rare disease[1].
Key Facts
- congenital stationary night blindness 1F's instance of is recorded as rare disease[2].
- congenital stationary night blindness 1F's instance of is recorded as class of disease[3].
- congenital stationary night blindness 1F's subclass of is recorded as congenital stationary night blindness[4].
- congenital stationary night blindness 1F's subclass of is recorded as genetic disease[5].
- congenital stationary night blindness 1F's OMIM ID is recorded as 615058[6].
- congenital stationary night blindness 1F's OMIM ID is recorded as 615058[7].
- congenital stationary night blindness 1F's Disease Ontology ID is recorded as DOID:0110864[8].
- congenital stationary night blindness 1F's genetic association is recorded as LRIT3[9].
- congenital stationary night blindness 1F's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110864[10].
- congenital stationary night blindness 1F's exact match is recorded as http://identifiers.org/doid/DOID:0110864[11].
- congenital stationary night blindness 1F's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_215[12].
- congenital stationary night blindness 1F's UMLS CUI is recorded as C3554399[13].
- congenital stationary night blindness 1F's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- congenital stationary night blindness 1F's Mondo ID is recorded as MONDO_0014026[15].
- congenital stationary night blindness 1F's UniProt disease ID is recorded as DI-03687[16].