Disease #06289 (DKCA6 (?Dyskeratosis congenita), OMIM:616553)

Official abbreviation DKCA6
Name ?Dyskeratosis congenita
OMIM ID 616553
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene ACD
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A

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