Humeroradial synostosis

Preferred Label : Humeroradial synostosis;

Type : Phenotype or locus, molecular basis unknown;

Included titles and symbols : Humeroradial/multiple synostosis syndrome;

Inheritance : Autosomal recessive;

Prefixed ID : %236400;

Détails

Origin ID

236400;

UMLS CUI

C2930865;

Automatic exact mappings (from CISMeF team)
- Humero-radial synostosis [ICD-11 Subcategory]
- Humeroradial fusion [HRDO Sign]
- humeroradial multiple synostosis syndrome [MeSH concept]
- humeroradial multiple synostosis syndrome [MeSH Supplementary Concept]
Currated CISMeF NLP mapping
- Humero-radial synostosis [ORDO Disease]
- Humeroradial synostosis [HPO term]
- Humeroradial synostosis (disorder) [SNOMED CT concept]
- humeroradial synostosis [DO Concept]
- ramer ladda syndrome [MeSH Supplementary Concept]
DO Cross reference
- humeroradial synostosis [DO Concept]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Brachycephaly [HPO term]
- Humeroradial synostosis [HPO term]
- Microtia [HPO term]
- Prominent forehead [HPO term]
- Renal insufficiency [HPO term]
- Small earlobe [HPO term]
- Wide nasal bridge [HPO term]
ORDO concept(s)
- Humero-radial synostosis [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Humeroradial synostosis [HPO term]
- Humeroradial synostosis (disorder) [SNOMED CT concept]
- Ramer Ladda syndrome [MeSH concept]
- ramer ladda syndrome [MeSH Supplementary Concept]

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

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