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DO Term : spondyloepimetaphyseal dysplasia with joint laxity type 3 [DOID:0112200] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A spondyloepimetaphyseal dysplasia with joint laxity characterized by multiple joint dislocations at birth, severe joint laxity, scoliosis, gracile metacarpals and metatarsals, delayed bone age, and poorly ossified carpal and tarsal bones that has_material_basis_in homozygous or compound heterozygous mutation in the EXOC6B gene on chromosome 2p13.2.
  • synonyms:
  • 618395,
  • OMIM:618395,
  • SEMDJL3
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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