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Metadata
ID DOID:0110333
Name Leber congenital amaurosis 7
Definition A Leber congenital amaurosis that has_material_basis_in mutation in the CRX gene on chromosome 19q13.
https://www.ncbi.nlm.nih.gov/pubmed/9537410
Xrefs

ICD10CM:H35.5

MIM:613829

Synonyms

LCA7 [EXACT]

Parent Relationships

is_a Leber congenital amaurosis

is_a monogenic disease

Subclass Logical Relationships

disease has basis in some gene

disease has basis in some Abnormality of prenatal development or birth

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