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DO Term : spondyloepimetaphyseal dysplasia, Genevieve-type [DOID:0080576] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A spondyloepimetaphyseal dysplasia that is characterized by infantile-onset severe developmental delay and skeletal dysplasia, including short stature, premature carpal ossification, platyspondyly, longitudinal metaphyseal striations, and small epiphyses and has_material_basis_in homozygous or compound heterozygous mutation in the NANS gene on chromosome 9q22.
  • synonyms:
  • GARD:10057,
  • OMIM:610442,
  • MESH:C535785,
  • ORDO:168454,
  • 610442
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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