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Links from OMIM

Items: 2

1.

Arrhythmogenic right ventricular dysplasia, familial, 15

MedGen UID:
1841324
Concept ID:
C5830688
Disease or Syndrome
2.

Cardiomyopathy, familial restrictive, 5

An autosomal dominant condition caused by mutation(s) in the FLNC gene, encoding filamin-C. It is characterized by restrictive cardiomyopathy in the context of normal contractility, left ventricular wall thickness and systolic function. [from NCI]

MedGen UID:
934715
Concept ID:
C4310748
Disease or Syndrome

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