Ichad syndrome

Preferred Label : Ichad syndrome;

Symbol : ICHAD;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Immunodysregulation, craniofacial anomalies, hearing impairment, athelia, and developmental delay;

Prefixed ID : #621234;

Details

Origin ID

621234;

Genes related to phenotype
- Ikaros family zinc finger 2 [OMIM gene]

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