Leber Congenital Amaurosis 3 (LCA3)

Alias:

Lca3

Retinitis Pigmentosa 94, Variable Age at Onset, Autosomal Recessive

Leber Congenital Amaurosis, Type 3

Leber Congenital Amaurosis Type 3

Rp94

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Leber Congenital Amaurosis 3, also known as lca3, is related to chronic interstitial cystitis and cone-rod dystrophy 17. An important gene associated with Leber Congenital Amaurosis 3 is SPATA7 (Spermatogenesis Associated 7), and among its related pathways/superpathways are Visual phototransduction and Ciliary landscape. Affiliated tissues include retina and eye, and related phenotypes are Increased viability and nervous system

Related ID：

MALACARDS：LBR013

OMIM：604232

MESH：C565814