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1.

Keutel syndrome

Keutel syndrome (KTLS) 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]

MedGen UID:
383722
Concept ID:
C1855607
Disease or Syndrome
2.

Cartilaginous ossification of nose

MedGen UID:
340915
Concept ID:
C1855616
Finding

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