Gollop-wolfgang complex

Preferred Label : Gollop-wolfgang complex;

Symbol : GWC;

CISMeF acronym : GWC;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Femur, unilateral bifid, with monodactylous ectrodactyly;

Inheritance : Autosomal recessive;

Prefixed ID : %228250;

Détails

Origin ID

228250;

UMLS CUI

C1856789;

Automatic exact mappings (from CISMeF team)
- Gollop-Wolfgang complex [MedDRA Preferred Term]
Currated CISMeF NLP mapping
- Bifid femur - monodactylous ectrodactyly [ICD-11 More detail]
- Bifid femur co-occurrent with monodactylous ectrodactyly (disorder) [SNOMED CT concept]
- Femur bifid with monodactylous ectrodactyly [MeSH concept]
- Gollop-Wolfgang complex [ORDO Disease]
- femur bifid with monodactylous ectrodactyly [MeSH Supplementary Concept]
HPO term(s)
- Absent tibia [HPO term]
- Aplasia of the ulna [HPO term]
- Autosomal recessive inheritance [HPO term]
- Bifid femur [HPO term]
- Foot monodactyly [HPO term]
- Hand monodactyly [HPO term]
- Split hand [HPO term]
ORDO concept(s)
- Gollop-Wolfgang complex [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Bifid femur co-occurrent with monodactylous ectrodactyly (disorder) [SNOMED CT concept]
- Femur bifid with monodactylous ectrodactyly [MeSH concept]
- Gollop-Wolfgang complex [ORDO Disease]
- Gollop-Wolfgang complex [MedDRA Preferred Term]
- femur bifid with monodactylous ectrodactyly [MeSH Supplementary Concept]

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