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GTR Home > Conditions/Phenotypes > Ulnar-mammary syndrome

Ulnar-mammary syndrome

Synonyms
PALLISTER ULNAR-MAMMARY SYNDROME; SCHINZEL SYNDROME; Ulnar-mammary syndrome of Pallister
Modes of inheritance
Autosomal dominant inheritance (Orphanet)

Summary

Ulnar-mammary syndrome (UMS) is an autosomal dominant disorder characterized by posterior limb deficiencies or duplications, apocrine/mammary gland hypoplasia and/or dysfunction, abnormal dentition, delayed puberty in males, and genital anomalies (Bamshad et al., 1996). [from OMIM]

Available tests

36 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (36 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: TBX3-ISO, UMS, XHL, TBX3
    Summary: T-box transcription factor 3

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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