non-syndromic pontocerebellar hypoplasia
Human disease
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non-syndromic pontocerebellar hypoplasia
Summary
non-syndromic pontocerebellar hypoplasia is a developmental defect during embryogenesis[1]. It is known by 7 alternative names across languages and contexts.[2]
Key Facts
- non-syndromic pontocerebellar hypoplasia's instance of is recorded as developmental defect during embryogenesis[3].
- non-syndromic pontocerebellar hypoplasia's instance of is recorded as class of disease[4].
- non-syndromic pontocerebellar hypoplasia is a type of neurodegeneration[5].
- non-syndromic pontocerebellar hypoplasia is a type of nervous system heredodegenerative disease[6].
- non-syndromic pontocerebellar hypoplasia is a type of posterior fossa malformation[7].
- non-syndromic pontocerebellar hypoplasia is a type of rare genetic developmental defect during embryogenesis[8].
- non-syndromic pontocerebellar hypoplasia's Commons category is recorded as Pontocerebellar hypoplasia[9].
- non-syndromic pontocerebellar hypoplasia's symptoms and signs is recorded as intellectual disability[10].
- non-syndromic pontocerebellar hypoplasia's health specialty is recorded as neurology[11].
- non-syndromic pontocerebellar hypoplasia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060264[12].
- non-syndromic pontocerebellar hypoplasia's exact match is recorded as http://identifiers.org/doid/DOID:0060264[13].
- non-syndromic pontocerebellar hypoplasia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_98523[14].
- non-syndromic pontocerebellar hypoplasia's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
Why It Matters
non-syndromic pontocerebellar hypoplasia is known by 7 alternative names across languages and contexts.[2]