Muscle hypertrophy

Preferred Label : Muscle hypertrophy;

Symbol : MSLHP;

CISMeF acronym : MSLHP;

Type : Phenotype, molecular basis known;

Prefixed ID : #614160;

Details

Origin ID

614160;

UMLS CUI

C0236033;

Automatic exact mappings (from CISMeF team)
- MSTN wt Allele [NCIt concept]
- Myostatin-related muscle hypertrophy [ORDO Disease]
- muscle symptom/complaint nos [ICPC-2 Rubric]
- myostatin-related muscle hypertrophy [DO Concept]
Currated CISMeF NLP mapping
- MUSCLE HYPERTROPHY [WHO-ART Preferred Term]
- Muscle hypertrophy [ICD-11 More detail]
- Muscle hypertrophy [MedDRA Preferred Term]
- Muscle hypertrophy [HRDO Sign]
- Muscle hypertrophy (finding) [SNOMED CT concept]
- Skeletal muscle hypertrophy [HPO term]
- muscle hypertrophy [GO term]
- muscular hypertrophy [Disease (Nov.)]
DO Cross reference
- myostatin-related muscle hypertrophy [DO Concept]
Genes related to phenotype
- Myostatin [OMIM gene]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Brisk reflexes [HPO term]
- Skeletal muscle hypertrophy [HPO term]
ORDO concept(s)
- Myostatin-related muscle hypertrophy [ORDO Disease]
Semantic type(s)
- Organ or Tissue Function [UMLS semantic type]
UMLS correspondences (same concept)
- MUSCLE HYPERTROPHY [WHO-ART Preferred Term]
- Muscle hypertrophy [MedDRA Preferred Term]
- Muscle hypertrophy (finding) [SNOMED CT concept]
- muscle hypertrophy [GO term]
- muscular hypertrophy [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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