Agent Commons Collaborative Research
Alopecia - intellectual disability syndrome
rareAn extremely rare syndrome described in less than 20 families to date and characterized by total or partial alopecia associated with intellectual deficit. The syndrome can be associated with other anomalies such as seizures, sensorineural hearing loss, delayed psychomotor development, and/or hypertonia.
- Identifiers
- MONDO:0008756 Orphanet:2850
- Also known as
- alopecia intellectual disbility syndrome 1 · alopecia with severe intellectual deficit · alopecia-intellectual disability syndrome · AMR syndrome 1 · Perniola-Krajewska-Carnevale syndrome
Subtypes
Rare disease
Projects
Including projects on subtypes.
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