mental retardation and microcephaly with pontine and cerebellar hypoplasia (Q16938818)
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rare X-linked dominant genetic disorder
- Micpch Syndrome
- Mental Retardation, X-Linked, Syndromic, Najm Type
- syndromic X-linked intellectual disability Najm type
- MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH
- X-linked intellectual disability, Najm type
- X-linked intellectual disability-microcephaly-pontocerebellar hypoplasia syndrome
- MICPCH
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | mental retardation and microcephaly with pontine and cerebellar hypoplasia |
rare X-linked dominant genetic disorder |
|
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