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DO Term : Native American myopathy [DOID:0060346] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A congenital myopathy that is characterized by congenital weakness, arthrogryposis, cleft palate, ptosis, myopathic facies, short stature, kykphoscoliosis, talipes deformities and susceptibility to malignant hyperthermia provoked by anesthesia and that has_material_basis_in homozygous mutation in the STAC3 gene on chromosome 12q13.
  • synonyms:
  • ORDO:168572,
  • UMLS_CUI:C1850625,
  • 255995,
  • congenital myopathy 13,
  • Bailey-Bloch congenital myopathy,
  • GARD:8432,
  • SNOMEDCT_US_2023_03_01:723439002,
  • MESH:C538343,
  • OMIM:255995
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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