C176924Level 11
Dyskeratosis Congenita, Autosomal Dominant 6
**Semantic type:** Disease or Syndrome
**Definition:** Dyskeratosis congenita caused by mutation(s) in the ACD gene, encoding adrenocortical dysplasia protein homolog.
**Synonyms:** - DKCA6 - DKCB7 - Dyskeratosis Congenita, Autosomal Recessive 7
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