ectodermal dysplasia, hypohidrotic, with hypothyroidism and agenesis of the corpus callosum

Preferred Label : ectodermal dysplasia, hypohidrotic, with hypothyroidism and agenesis of the corpus callosum;

Origin ID

C565605;

UMLS CUI

C1857053;

Automatic exact mappings (from CISMeF team)
- Ectodermal dysplasia, hypohidrotic, with hypothyroidism and agenesis of the corpus callosum [OMIM Phenotype]
MeSH term(s) associated for indexing
- agenesis of corpus callosum [MeSH Descriptor]
- congenital hypothyroidism [MeSH Descriptor]
- ectodermal dysplasia [MeSH Descriptor]
- intellectual disability [MeSH Descriptor]
Record concept(s)
- ectodermal dysplasia, hypohidrotic, with hypothyroidism and agenesis of the corpus callosum [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Ectodermal dysplasia, hypohidrotic, with hypothyroidism and agenesis of the corpus callosum [OMIM Phenotype]
- Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome [ORDO Disease]