|OBO ID: DOID:0060614|
|Term Name:||ulnar-mammary syndrome||Search Ontology:|
|Definition:||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. (2)|
|Ontology:||Human Disease (DOID:0060614)|
|is a type of:||
OTHER ulnar-mammary syndrome PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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