Disease #07115 (CORD14 (cone-rod dystrophy, type 14), OMIM:620342)

Official abbreviation CORD14
Name cone-rod dystrophy, type 14
OMIM ID 620342
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene UNC119
Associated tissues -
Disease features -
Remarks -
Date created 2024-11-11 21:35:31 +01:00 (CET)
Date last edited N/A

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