DO_rare_slim has material basis in autosomal dominant disease ulnar-mammary syndrome ORDO:3138 DOID:0060614 disease_ontology SNOMEDCT_US_2025_09_01:700211007 UMLS_CUI:C1866994 A syndrome that is characterized by posterior limb deficiencies or duplications, apocrine/mammary gland hypoplasia and, or dysfunction, abnormal dentition, delayed puberty in males, and genital anomalies and that has_material_basis_in heterozygous mutation in the TBX3 gene. MESH:C536937 GARD:118 MIM:181450 Pallister ulnar-mammary syndrome Schinzel syndrome syndrome autosomal dominant inheritance