Ogden Syndrome

Preferred Label : Ogden Syndrome;

NCIt synonyms : OGDNS;

NCIt definition : An X-linked condition caused by mutation(s) in the NAA10 gene, encoding N-alpha-acetyltransferase 10. It is characterized by characterized by postnatal growth failure, severely delayed psychomotor development, variable dysmorphic facial features, and hypotonia.;

Details

Origin ID

C188215;

UMLS CUI

C3275447;

Currated CISMeF NLP mapping
- Ogden syndrome [MedDRA Preferred Term]
- Ogden syndrome [DO Concept]
- Ogden syndrome [OMIM Phenotype]
- Ogden syndrome [ORDO Disease]
- Ogden syndrome (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Ogden syndrome [OMIM Phenotype]
- Ogden syndrome [MedDRA Preferred Term]
- Ogden syndrome (disorder) [SNOMED CT concept]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
disease_mapped_to_gene
- NAA10 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients