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DO Term : Smith-McCort dysplasia 1 [DOID:0081270] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A Smith-McCort dysplasia that is characterized by short limbs and a short trunk with a barrel-shaped chest and has_material_basis_in homozygous or compound heterozygous mutation in the DYM gene (607461) on chromosome 18q21.
  • synonyms:
  • OMIM:607326,
  • 607326
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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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