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DO Term : Pierpont syndrome [DOID:0081362] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  An autosomal dominant intellectual developmental disorder that is characterized by distinctive facial characteristics, especially when smiling, plantar fat pads, and other limb anomalies and that has_material_basis_in heterozygous mutation in the TBL1XR1 gene on chromosome 3q26.
  • synonyms:
  • Plantar lipomatosis-unusual facies-developmental delay syndrome,
  • OMIM:602342,
  • ORDO:487825,
  • 602342,
  • Plantar lipomatosis-facial dysmorphism-developmental delay syndrome
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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