MedGen for OMIM (Select 126141) - MedGen - NCBI

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Items: 2

Select item 8993891.

Intellectual disability, autosomal dominant 33

Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the DPP6 gene. [from MONDO]

MedGen UID:: 899389
•Concept ID:: C4225375
•: Mental or Behavioral Dysfunction

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Select item 4428232.

Ventricular fibrillation, paroxysmal familial, 2

Any ventricular fibrillation in which the cause of the disease is a mutation in the DPP6 gene. [from MONDO]

MedGen UID:: 442823
•Concept ID:: C2751829
•: Disease or Syndrome

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MedGen for OMIM (Select 126141) (2)
MedGen
A-type potassium channel modulatory protein DPP6 isoform X1 [Homo sapiens]
A-type potassium channel modulatory protein DPP6 isoform X1 [Homo sapiens]
gi|2462612700|ref|XP_054213391.1|

Protein

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