Hypomelia with mullerian duct anomalies

Preferred Label : Hypomelia with mullerian duct anomalies;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Limb-uterus syndrome;

Inheritance : Autosomal dominant;

Prefixed ID : 146160;

Détails

Origin ID

146160;

UMLS CUI

C1840335;

Automatic exact mappings (from CISMeF team)
- Hypomelia mullerian duct anomalies [MeSH concept]
- hypomelia mullerian duct anomalies [MeSH Supplementary Concept]
Currated CISMeF NLP mapping
- Mullerian duct anomalies - limb anomalies [ICD-11 More detail]
- Müllerian duct anomalies-limb anomalies syndrome [ORDO Disease]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Longitudinal vaginal septum [HPO term]
- Postaxial hand polydactyly [HPO term]
- Split hand [HPO term]
- Uterus didelphys [HPO term]
ORDO concept(s)
- Müllerian duct anomalies-limb anomalies syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hypomelia mullerian duct anomalies [MeSH concept]
- Mullerian duct anomalies - limb anomalies [ICD-11 More detail]
- Müllerian duct anomalies-limb anomalies syndrome [ORDO Disease]
- hypomelia mullerian duct anomalies [MeSH Supplementary Concept]

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

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