Search Ontology:
Human Disease

autosomal recessive isolated ectopia lentis 2

Term ID
DOID:0111149
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
Ontology
Human Disease   ( DOID:0111149 )
Relationships
is a type of
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Genes Involved
Zebrafish Models