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DO Term : MEND syndrome [DOID:0111865] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A lipid metabolism disorder characterized by a defect in sterol biosynthesis that results in variable features including intellectual disability, short stature, scoliosis, digital abnormalities, cataracts, and dermatologic abnormalities that has_material_basis_in hemizygous mutation in EBP on chromosome Xp11.23.
  • synonyms:
  • 300960,
  • ORDO:401973,
  • male EBP disorder with neurological defects,
  • UMLS_CUI:C4085243,
  • OMIM:300960
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Ontology Term --> All ancestors

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Ontology Term --> Direct children

Ontology Term --> Direct parents