Aarskog syndrome

Preferred Label : Aarskog syndrome;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0529792;

UMLS CUI

C0175701;

Automatic exact mappings (from CISMeF team)
- Autosomal recessive faciodigitogenital syndrome [ORDO Disease]
- Congenital malformation syndromes predominantly associated with short stature [ICD-10 Sub-category]
- Congenital malformation syndromes predominantly associated with short stature [ICD-10 Sub-category (who)]
- Greig's syndrome [MedDRA Preferred Term]
Currated CISMeF NLP mapping
- Aarskog Syndrome [NCIt concept]
- Aarskog syndrome [Disease (Nov.)]
- Aarskog syndrome [MedDRA LLT]
- Aarskog syndrome [DO Concept]
- Aarskog syndrome (disorder) [SNOMED CT concept]
- Aarskog-Scott syndrome [ICD-11 More detail]
- Aarskog-Scott syndrome [ORDO Disease]
- Aarskog-Scott syndrome [MedDRA LLT]
- Aarskog-scott syndrome [OMIM Phenotype]
- X-linked Aarskog syndrome [DO Concept]
- aarskog syndrome [SNOMED Notion]
Related MeSH concept(s)
- faciodigitogenital syndrome, recessive [MeSH concept]
Related record
- Aarskog syndrome [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Aarskog Syndrome [NCIt concept]
- Aarskog syndrome [MedDRA LLT]
- Aarskog syndrome (disorder) [SNOMED CT concept]
- Aarskog-Scott syndrome [MedDRA LLT]
- Aarskog-Scott syndrome [ORDO Disease]
- Aarskog-scott syndrome [OMIM Phenotype]
- X-linked Aarskog syndrome [DO Concept]
- aarskog syndrome [SNOMED Notion]