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Diseases
Genes (2224)
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ABHD5
Cerebral Creatine Deficiency
HMBS
Acute Intermittent Porphyria
Childhood Leukemia
TTPA
Familial Isolated Vitamin E Deficiency
GAMT
Guanidinoacetate Methyltransferase Deficiency
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
TRNL1
Merrf Syndrome
LIPA
Acid Lipase Disease
TRNP
Merrf Syndrome
TRNF
Merrf Syndrome
IL1B
Alopecia, Androgenetic, 1
Merrf Syndrome
Ophthalmia
Renpenning's Syndrome
Childhood Leukemia
Cystinosis
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
DMPK
Myotonic Dystrophy
ASS1
Citrullinemia Type I
BRCA1
Primary Peritoneal Carcinoma
Childhood Leukemia
PRKAR1A
Alopecia, Androgenetic, 1
Enamel-Renal Syndrome
Childhood Leukemia
AR
Alopecia, Androgenetic, 1
Tetraplegia
Childhood Leukemia