Aurocephalosyndactyly

Preferred Label : Aurocephalosyndactyly;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : AURALCEPHALOSYNDACTYLY;

Inheritance : Autosomal dominant;

Prefixed ID : 109050;

Details

Origin ID

109050;

UMLS CUI

C1862380;

Automatic exact mappings (from CISMeF team)
- Aurocephalosyndactyly [ICD-11 More detail]
Currated CISMeF NLP mapping
- Aurocephalosyndactyly [ORDO Disease]
- aurocephalosyndactyly [MeSH concept]
- aurocephalosyndactyly [MeSH Supplementary Concept]
HPO term(s)
- 4-5 toe syndactyly [HPO term]
- Abnormality of cardiovascular system morphology [HPO term]
- Autosomal dominant inheritance [HPO term]
- Craniosynostosis [HPO term]
- Hearing impairment [HPO term]
- Intellectual disability, mild [HPO term]
- Short columella [HPO term]
ORDO concept(s)
- Aurocephalosyndactyly [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- aurocephalosyndactyly [MeSH Supplementary Concept]
- aurocephalosyndactyly [MeSH concept]

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