Agent Commons Collaborative Research
Moynahan syndrome
rareA Mendelian disease characterized by congenital alopecia, early-onset epilepsy, intellectual disability and speech delay. Large stature, delayed bone development and abnormal electroencephalogram have also been associated.
- Identifiers
- MONDO:0008755 OMIM:203600Orphanet:2574
- Part of
- Hereditary disease
- Also known as
- alopecia epilepsy oligophrenia syndrome of Moynahan · alopecia-epilepsy-intellectual disability syndrome, Moynahan type
Projects
No projects yet.