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Diseases
Genes (1098)
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POLG
Anemia
Balo Concentric Sclerosis
TTPA
Familial Isolated Vitamin E Deficiency
SLC12A6
Andermann Syndrome
PQBP1
Renpenning's Syndrome
IFIH1
Singleton Merten Syndrome
Anemia
SLC17A5
Anemia
Salla Disease
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
NGLY1
Ngly1 Deficiency
UBE3B
Kaufman Oculocerebrofacial Syndrome
HAMP
Anemia
ACTG2
Berdon Syndrome
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
ASS1
Citrullinemia Type I
MYH11
Berdon Syndrome
MYLK
Berdon Syndrome
GATA1
Melorheostosis
Anemia
EPO
Anemia
Salla Disease
CTNS
Cystinosis
REN
Anemia