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Diseases
Genes (1042)
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ABHD5
Cerebral Creatine Deficiency
POLG
Balo Concentric Sclerosis
SLC6A19
Hartnup Disease
GAMT
Guanidinoacetate Methyltransferase Deficiency
TTPA
Familial Isolated Vitamin E Deficiency
OPA3
Costeff Syndrome
SLC17A5
Salla Disease
ABCC9
Cantú Syndrome
PQBP1
Renpenning's Syndrome
UMOD
Medullary Cystic Kidney Disease
TAF1
Dystonia 3, Torsion, X-Linked
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
KCNJ8
Cantú Syndrome
Enamel-Renal Syndrome
IFIH1
Singleton Merten Syndrome
IDH1
Ollier Disease
FLNA
Intestinal Neuronal Dysplasia
Bronchopulmonary Dysplasia
Fg Syndrome
IDH2
Ollier Disease
IL1B
Alopecia, Androgenetic, 1
Bronchopulmonary Dysplasia
Alexithymia
Systemic Inflammatory Response Syndrome
Renpenning's Syndrome
Back Pain
Cystinosis