chromosome 13q14 deletion syndrome (DOID:0060391)
Alliance: disease page
Synonyms: deletion 13q14
Alt IDs: OMIM:613884, ICD10CM:Q93.5, ORDO:1587
Definition: A chromosomal deletion syndrome that is characterized by low birth weight, dysmorphic facies, limb defects, genital malformations and psychomotor developmental delay, has_material_basis_in deletion of the long arm of chromosome 13.