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LMNA
- Werner Syndrome
- Cardiomyopathy, Dilated, 1g
- Myoclonic Epilepsy Of Unverricht And Lundborg
- Hutchinson-Gilford Progeria Syndrome
ABHD5
- Cerebral Creatine Deficiency
WRN
- Werner Syndrome
- Hutchinson-Gilford Progeria Syndrome
GAMT
- Guanidinoacetate Methyltransferase Deficiency
CSTB
- Myoclonic Epilepsy Of Unverricht And Lundborg
MYO15A
- Deafness, Autosomal Recessive 3
ZMPSTE24
- Hutchinson-Gilford Progeria Syndrome
UMOD
- Medullary Cystic Kidney Disease
PITX3
- Anterior Segment Dysgenesis 1
TTN
- Cardiomyopathy, Dilated, 1g
HMGB3
- Microphthalmia, Syndromic 13
FOXE3
- Anterior Segment Dysgenesis 1
TP53
- Epithelioid Hemangioendothelioma
- Disseminated Superficial Actinic Porokeratosis
- Leukemia, Chronic Lymphocytic, Susceptibility To, 2
- Alopecia, Androgenetic, 1
- Werner Syndrome
- Hutchinson-Gilford Progeria Syndrome
RBM20
- Cardiomyopathy, Dilated, 1g
TFE3
- Epithelioid Hemangioendothelioma
- Vascular Tumor
WWTR1
- Epithelioid Hemangioendothelioma
CAMTA1
- Epithelioid Hemangioendothelioma
SRD5A2
- Alopecia, Androgenetic, 1
TNNT2
- Cardiomyopathy, Dilated, 1g
SCN5A
- Cardiomyopathy, Dilated, 1g