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 ...