GTR Home > Conditions/Phenotypes > Keutel syndrome


Keutal syndrome is an autosomal recessive disorder characterized by multiple peripheral pulmonary stenoses, brachytelephalangy, inner ear deafness, and abnormal cartilage ossification or calcification (summary by Khosroshahi et al., 2014). [from OMIM]

Available tests

12 tests are in the database for this condition.

Check Associated genes and Related conditions for additional relevant tests.

Associated genes


Clinical features


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