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Diseases
Genes (1156)
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SLC6A19
Hartnup Disease
POLG
Balo Concentric Sclerosis
TTPA
Familial Isolated Vitamin E Deficiency
BLM
Bloom Syndrome
OPA3
Costeff Syndrome
IRF6
Van Der Woude Syndrome
SLC17A5
Salla Disease
FECH
Erythropoietic Protoporphyria
UMOD
Medullary Cystic Kidney Disease
Van Der Woude Syndrome
MED12
Fg Syndrome
ABCC9
Cantú Syndrome
GRHL3
Van Der Woude Syndrome
PMM2
Pmm2 Deficiency
SYNE1
Bronchopulmonary Dysplasia
Emery–dreifuss Muscular Dystrophy
LMNA
Emery–dreifuss Muscular Dystrophy
IFIH1
Chronic Periodontitis
Singleton Merten Syndrome
NOP56
Spinocerebellar Ataxia Type 36
FLNA
Intestinal Neuronal Dysplasia
Bronchopulmonary Dysplasia
Fg Syndrome
Emery–dreifuss Muscular Dystrophy
KCNJ8
Cantú Syndrome
IL1B
Bronchopulmonary Dysplasia
Cystinosis
Chronic Periodontitis
Van Der Woude Syndrome