ZFIN Human Disease: Leber congenital amaurosis 15

OBO ID: DOID:0110189

OBO ID: DOID:0110189

Term Name:	Leber congenital amaurosis 15	Search Ontology:
Synonyms:	LCA15
Definition:	A Leber congenital amaurosis that has_material_basis_in mutation in the TULP1 gene on chromosome 6p21.3. https://www.ncbi.nlm.nih.gov/pubmed/15024725
References:	ICD10CM:H35.5 OMIM:613843
Ontology:	Human Disease ( DOID:0110189 )

Relationships

is a type of:	autosomal recessive disease Leber congenital amaurosis autosomal recessive disease Leber congenital amaurosis Show first 5 Terms

OTHER Leber congenital amaurosis 15 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
TULP1	tulp1b tulp1a	Leber congenital amaurosis 15	613843

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None