N syndrome - CISMeF

Preferred Label : N syndrome;

Symbol : NSX;

CISMeF acronym : NSX;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : X-linked;

Prefixed ID : 310465;

Details

Origin ID

310465;

UMLS CUI

C2936859;

Currated CISMeF NLP mapping
- N syndrome [DO Concept]
- N syndrome [ICD-11 More detail]
- N syndrome [MeSH concept]
- N syndrome [MeSH Supplementary Concept]
- N syndrome [ORDO Disease]
- N syndrome (disorder) [SNOMED CT concept]
DO Cross reference
- N syndrome [DO Concept]
HPO term(s)
- Abnormality of chromosome stability [HPO term]
- Cryptorchidism [HPO term]
- Deafness [HPO term]
- Hearing impairment [HPO term]
- Hypospadias [HPO term]
- Intellectual disability [HPO term]
- Leukemia [HPO term]
- Neoplasm [HPO term]
- Spasticity [HPO term]
- Visual impairment [HPO term]
- X-linked inheritance [HPO term]
ORDO concept(s)
- N syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- N syndrome [MeSH concept]
- N syndrome [MeSH Supplementary Concept]
- N syndrome [ORDO Disease]
- N syndrome [DO Concept]
- N syndrome (disorder) [SNOMED CT concept]

Keyword's position in hierarchy(ies) :

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