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Items: 2

1.

Retinitis pigmentosa 40

Any retinitis pigmentosa in which the cause of the disease is a mutation in the PDE6B gene. [from MONDO]

MedGen UID:
462457
Concept ID:
C3151107
Disease or Syndrome
2.

Congenital stationary night blindness autosomal dominant 2

Any congenital stationary night blindness in which the cause of the disease is a mutation in the PDE6B gene. [from MONDO]

MedGen UID:
361814
Concept ID:
C1876182
Disease or Syndrome

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