Cerebellar hypoplasia with endosteal sclerosis

Preferred Label : Cerebellar hypoplasia with endosteal sclerosis;

Obsolete resource : true;

Moved to : 614381;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal recessive;

Prefixed ID : 213002;

Details

Origin ID

213002;

UMLS CUI

C1859301;

Currated CISMeF NLP mapping
- Cerebellar hypoplasia with endosteal sclerosis [MeSH concept]
- Endosteal sclerosis - cerebellar hypoplasia [ICD-11 More detail]
- Endosteal sclerosis-cerebellar hypoplasia syndrome [ORDO Disease]
- cerebellar hypoplasia with endosteal sclerosis [MeSH Supplementary Concept]
ORDO concept(s)
- Endosteal sclerosis-cerebellar hypoplasia syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cerebellar hypoplasia with endosteal sclerosis [MeSH concept]
- Endosteal sclerosis-cerebellar hypoplasia syndrome [ORDO Disease]
- cerebellar hypoplasia with endosteal sclerosis [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

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