Amelogenesis imperfecta, hypoplastic-hypomaturation, X-linked 2

Preferred Label : Amelogenesis imperfecta, hypoplastic-hypomaturation, X-linked 2;

CISMeF synonym : amelogenesis imperfecta, hypoplastic/hypomaturation, X-linked 2;

UMLS semantic type : T047 - Disease or Syndrome;

Details

Origin ID

M0532705;

UMLS CUI

C1845051;

Currated CISMeF NLP mapping
- Amelogenesis imperfecta, hypoplastic/hypomaturation, X-linked 2 [OMIM Phenotype]
- X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 [DO Concept]
Related record
- burnett schwartz berberian syndrome [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Amelogenesis imperfecta, hypoplastic/hypomaturation, X-linked 2 [OMIM Phenotype]
- X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 [DO Concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients