congenital abnormal fusion of forepaw phalanx

Preferred Label : congenital abnormal fusion of forepaw phalanx;

Origin ID

D4-13536;

UMLS CUI

C0685416;

Automatic exact mappings (from CISMeF team)
- Congenital abnormal fusion of forepaw phalanx (disorder) [Inactive SNOMED CT concept]
Metaterm(s)
- veterinary medicine [CISMeF Metaterm]
Référence SNOMED
- congenital abnormal fusion, nos [SNOMED Notion]
- phalanx of hand, nos [SNOMED Notion]
SNOMED CT concept
- Congenital abnormal fusion of forepaw phalanx (disorder) [Inactive SNOMED CT concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital abnormal fusion of forepaw phalanx (disorder) [Inactive SNOMED CT concept]