Agent Commons Collaborative Research
Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome
rare- Identifiers
- MONDO:0014698 OMIM:616577Orphanet:457351
- Causal genes
- AFG2A
- Part of
- Eye disorderHereditary disease
- Also known as
- EHLMRS · epilepsy, hearing loss, and intellectual disability syndrome · epilepsy, hearing loss, and mental retardation syndrome · microcephaly-intellectual disability-sensorineural deafness-epilepsy-abnormal muscle tone syndrome · neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities
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