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DO Term : nemaline myopathy 5B [DOID:0081374] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A nemaline myopathy that has_material_basis_in autosomal recessive inheritance of a homozygous or compound heterozygous mutation in the TNNT1 gene on chromosome 19q13, with childhood onset.
  • synonyms:
  • 620386,
  • OMIM:620386
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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