myelodysplasia, immunodeficiency, facial dysmorphism, short stature, and psychomotor delay

Preferred Label : myelodysplasia, immunodeficiency, facial dysmorphism, short stature, and psychomotor delay;

Origin ID

C563345;

UMLS CUI

C1832442;

Currated CISMeF NLP mapping
- Myelodysplasia, immunodeficiency, facial dysmorphism, short stature, and psychomotor delay [OMIM Phenotype]
MeSH term(s) associated for indexing
- craniofacial abnormalities [MeSH Descriptor]
- growth disorders [MeSH Descriptor]
- immunologic deficiency syndromes [MeSH Descriptor]
- myelodysplastic syndromes [MeSH Descriptor]
- psychomotor disorders [MeSH Descriptor]
Record concept(s)
- myelodysplasia, immunodeficiency, facial dysmorphism, short stature, and psychomotor delay [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Myelodysplasia, immunodeficiency, facial dysmorphism, short stature, and psychomotor delay [OMIM Phenotype]