Hydrocephalus, autosomal dominant

Preferred Label : Hydrocephalus, autosomal dominant;

Symbol : HDCPH1;

CISMeF acronym : HDCPH1;

Type : Phenotype or locus, molecular basis unknown;

Inheritance : Autosomal dominant;

Prefixed ID : %123155;

Details

Origin ID

123155;

UMLS CUI

C1838347;

Currated CISMeF NLP mapping
- Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome [ORDO Disease]
- hydrocephalus, autosomal dominant [MeSH concept]
- hydrocephalus, autosomal dominant [MeSH Supplementary Concept]
DO Cross reference
- hydrocephalus [DO Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Cerebellar vermis hypoplasia [HPO term]
- Dandy-Walker malformation [HPO term]
- Hydrocephalus [HPO term]
- Posterior fossa cyst [HPO term]
- Sagittal craniosynostosis [HPO term]
ORDO concept(s)
- Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome [ORDO Disease]
- hydrocephalus, autosomal dominant [MeSH Supplementary Concept]
- hydrocephalus, autosomal dominant [MeSH concept]

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