Disease-gene associations mined from literature

Human genes for ulnar-mammary syndrome

Ulnar-mammary syndrome [DOID:0060614]

A syndrome that has_material_basis_in heterozygous mutation in the TBX3 gene. It is characterized by posterior limb deficiencies or duplications, apocrine/mammary gland hypoplasia and, or dysfunction, abnormal dentition, delayed puberty in males, and genital anomalies.

Synonyms:  ulnar-mammary syndrome,  DOID:0060614,  ulnarmammary syndrome,  ulnar-mammary disease,  ulnar-mammary disorder ...