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Items: 4

1.

Deafness, autosomal dominant 13

MedGen UID:
400917
Concept ID:
C1866095
Disease or Syndrome
2.

Ear without helix

MedGen UID:
343678
Concept ID:
C1851899
Finding
3.

Loss of Chromosome 6p

MedGen UID:
274707
Concept ID:
C1517987
Cell or Molecular Dysfunction
4.

Deafness, autosomal dominant 23

MedGen UID:
343162
Concept ID:
C1854594
Disease or Syndrome
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