Cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay

Preferred Label : Cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay;

Symbol : CCDDRD;

Type : Phenotype, molecular basis known;

Prefixed ID : #620469;

Détails

Origin ID

620469;

UMLS CUI

C5882675;

Genes related to phenotype
- Neurogenin 1 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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