Medical Subject Headings

Last uploaded: November 5, 2019
Preferred Name

Nemaline myopathy 1

Synonyms

Nemaline myopathy caused by mutation in the tropomyosin 3 gene

ID

http://purl.bioontology.org/ontology/MESH/C538348

altLabel

Nemaline myopathy caused by mutation in the tropomyosin 3 gene

Cap Myopathy, Tpm3-Related

cui

C1836448

C2750414

HM

D017696

Inverse of RB

0

Mapped to

http://purl.bioontology.org/ontology/MESH/D017696

MDA

20100825

MeSH Frequency

0

MMR

20121105

notation

C538348

prefLabel

Nemaline myopathy 1

SC

3

TERMUI

T810854

T745518

T745520

TH

ORD (2010)

OMIM (2013)

tui

T047

Delete Subject Author Type Created
No notes to display
Create New Mapping

Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/OMIM/191030 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/609284 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/609284 Online Mendelian Inheritance in Man LOOM
http://purl.obolibrary.org/obo/DOID_0110926 Human Disease Ontology 123 LOOM