Myosin, heavy chain 3, skeletal muscle, embryonic

Preferred Label : Myosin, heavy chain 3, skeletal muscle, embryonic;

Symbol : MYH3;

CISMeF acronym : MYH3;

Type : Gene;

Alternative titles and symbols : Myosin, skeletal, heavy chain, embryonic 1; MYHSE1; MYHC-EMB;

Ensembl ID : ENSG00000109063;

Prefixed ID : *160720;

Details

Origin ID

160720;

UMLS CUI

C1417538;

Automatic exact mappings (from CISMeF team)
- myosin heavy chain 3 [ORDO Gene]
- myosin heavy chain 3 [HGNC gene]
HGNC gene
- myosin heavy chain 3 [HGNC gene]
NCIt concept(s)
- MYH3 Gene [NCIt concept]
- MYH3 wt Allele [NCIt concept]
- Myosin-3 [NCIt concept]
ORDO concept(s)
- myosin heavy chain 3 [ORDO Gene]
Phenotypes related
- Arthrogryposis, distal, type 2a [OMIM Phenotype]
- Arthrogryposis, distal, type 2b3 [OMIM Phenotype]
- Contractures, pterygia, and spondylocarpotarsal fusion syndrome 1a [OMIM Phenotype]
- Contractures, pterygia, and spondylocarpotarsal fusion syndrome 1b [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- MYH3 Gene [NCIt concept]
- myosin heavy chain 3 [HGNC gene]

Keyword's position in hierarchy(ies) :

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