Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019
Preferred Name

TROPOMYOSIN 3

Synonyms

ALPHA-TROPOMYOSIN 3

ID

http://purl.bioontology.org/ontology/OMIM/191030

altLabel

ALPHA-TROPOMYOSIN 3

MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION

NEMALINE MYOPATHY 1

TPM3

TRK ONCOGENE

CAP MYOPATHY 1

TPM3/NTRK1 FUSION GENE

ALPHA-TROPOMYOSIN, SLOW SKELETAL

cui

C3714994

C1836448

C0546264

C1420874

Gene Locus

1q22-q23

Gene Symbol

CFTD

TPM3

CAPM1

NEM1

Has allelic variant

http://purl.bioontology.org/ontology/OMIM/191030.0003

http://purl.bioontology.org/ontology/OMIM/191030.0010

http://purl.bioontology.org/ontology/OMIM/191030.0011

http://purl.bioontology.org/ontology/OMIM/191030.0002

http://purl.bioontology.org/ontology/OMIM/191030.0004

http://purl.bioontology.org/ontology/OMIM/191030.0005

http://purl.bioontology.org/ontology/OMIM/191030.0009

http://purl.bioontology.org/ontology/OMIM/191030.0001

http://purl.bioontology.org/ontology/OMIM/191030.0006

http://purl.bioontology.org/ontology/OMIM/191030.0008

http://purl.bioontology.org/ontology/OMIM/191030.0007

MIMTYPEMEANING

Gene with known sequence

Moved from

164970

notation

191030

OMIM Entry Type

1

OMIM MimType Value

star

prefLabel

TROPOMYOSIN 3

tui

T028

T019

T047

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http://purl.bioontology.org/ontology/MESH/C538348 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/ICD10CM/G71.2 International Classification of Diseases, Version 10 - Clinical Modification CUI
http://purl.bioontology.org/ontology/MESH/D020914 Medical Subject Headings CUI