alobar holoprosencephaly

Preferred Label : alobar holoprosencephaly;

UMLS semantic type : T019 - Congenital Abnormality;

Origin ID

M0336860;

UMLS CUI

C0431363;

Automatic exact mappings (from CISMeF team)
- Alobar holoprosencephaly [ICD-11 More detail]
- alobar holoprosencephaly [Radlex concept]
Currated CISMeF NLP mapping
- Alobar holoprosencephaly [HPO term]
- Alobar holoprosencephaly [ORDO Disease]
- Alobar holoprosencephaly (disorder) [SNOMED CT concept]
Related record
- holoprosencephaly [MeSH Descriptor]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Alobar holoprosencephaly [ORDO Disease]
- Alobar holoprosencephaly [HPO term]
- Alobar holoprosencephaly (disorder) [SNOMED CT concept]