ZFIN Human Disease: autosomal recessive isolated ectopia lentis 2

OBO ID: DOID:0111149

OBO ID: DOID:0111149

Term Name:	autosomal recessive isolated ectopia lentis 2	Search Ontology:
Synonyms:	ECTOL2
Definition:	An isolated ectopia lentis that has_material_basis_in homozygous or compound heterozygous mutation in the ADAMTSL4 gene on chromosome 1q21. (2)
References:	OMIM:225100
Ontology:	Human Disease ( DOID:0111149 )

Relationships

is a type of:	autosomal recessive disease isolated ectopia lentis autosomal recessive disease isolated ectopia lentis Show first 5 Terms

OTHER autosomal recessive isolated ectopia lentis 2 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
ADAMTSL4	adamtsl4	Ectopia lentis, isolated, autosomal recessive	225100

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None