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Items: 3

1.

Tooth agenesis, selective, 3

Any tooth agenesis in which the cause of the disease is a mutation in the PAX9 gene. [from MONDO]

MedGen UID:
410035
Concept ID:
C1970291
Disease or Syndrome
2.

Hypotrichosis 13

Any hypotrichosis in which the cause of the disease is a mutation in the KRT71 gene. [from MONDO]

MedGen UID:
863053
Concept ID:
C4014616
Disease or Syndrome
3.

Abnormal skin morphology

Any morphological abnormality of the skin. [from HPO]

MedGen UID:
869110
Concept ID:
C4023528
Anatomical Abnormality
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