Fg syndrome 3 - CISMeF

Preferred Label : Fg syndrome 3;

Symbol : FGS3;

CISMeF acronym : FGS3;

Type : Phenotype or locus, molecular basis unknown;

Description : For a general phenotypic description and a discussion of genetic heterogeneity of FG syndrome, see FGS1 (305450).;

Prefixed ID : %300406;

Details

Origin ID

300406;

UMLS CUI

C1845567;

Broader ORDO disease(s)
- FG syndrome [ORDO Disease]
Currated CISMeF NLP mapping
- FG syndrome 3 [MeSH concept]
DO Cross reference
- FG syndrome [DO Concept]
ORDO concept(s)
- FG syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- FG syndrome 3 [MeSH concept]

Keyword's position in hierarchy(ies) :

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