mental retardation with optic atrophy, facial dysmorphism, microcephaly, and short stature

Preferred Label : mental retardation with optic atrophy, facial dysmorphism, microcephaly, and short stature;

Origin ID

C563810;

UMLS CUI

C1836915;

Automatic exact mappings (from CISMeF team)
- Mental retardation with optic atrophy, facial dysmorphism, microcephaly, and short stature [OMIM Phenotype]
MeSH term(s) associated for indexing
- craniofacial abnormalities [MeSH Descriptor]
- growth disorders [MeSH Descriptor]
- intellectual disability [MeSH Descriptor]
- optic atrophy [MeSH Descriptor]
Record concept(s)
- mental retardation with optic atrophy, facial dysmorphism, microcephaly, and short stature [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Mental retardation with optic atrophy, facial dysmorphism, microcephaly, and short stature [OMIM Phenotype]