Craniosynostosis, adelaide type

Preferred Label : Craniosynostosis, adelaide type;

Symbol : CRSA;

CISMeF acronym : CRSA;

Type : Phenotype or locus, molecular basis unknown;

Inheritance : ? Autosomal dominant (4p16);

Prefixed ID : %600593;

Détails

Origin ID

600593;

UMLS CUI

C1833578;

Automatic exact mappings (from CISMeF team)
- Syndromic craniosynostosis [ORDO Disease]
- crisamicin A [MeSH Supplementary Concept]
Currated CISMeF NLP mapping
- craniosynostosis, adelaide type [MeSH concept]
- craniosynostosis, adelaide type [MeSH Supplementary Concept]
DO Cross reference
- craniosynostosis [DO Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Carpal bone malsegmentation [HPO term]
- Cone-shaped epiphyses of the phalanges of the hand [HPO term]
- Cone-shaped epiphyses of the toes [HPO term]
- Coned epiphyses of hands and feet [HPO term]
- Craniosynostosis [HPO term]
- Hallux valgus [HPO term]
- Shortening of all distal phalanges of the fingers [HPO term]
- Shortening of all middle phalanges of the fingers [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- craniosynostosis, adelaide type [MeSH Supplementary Concept]
- craniosynostosis, adelaide type [MeSH concept]

Position du mot-clé dans l'(les) arborescence(s) :

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