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Diseases
Genes (786)
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ABHD5
Cerebral Creatine Deficiency
TTPA
Familial Isolated Vitamin E Deficiency
GAMT
Guanidinoacetate Methyltransferase Deficiency
COL2A1
Collagen, Type Ii, Alpha-1
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
ALK
Inflammatory Myofibroblastic Tumour
Vascular Tumor
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Hepatitis E
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
DMPK
Myotonic Dystrophy
FLNA
Influenza-Like Illness
Intestinal Neuronal Dysplasia
Fg Syndrome
RANBP2
Cholera
Inflammatory Myofibroblastic Tumour
PAH
Phenylketonuria
ASS1
Citrullinemia Type I
MYH11
Berdon Syndrome
MYLK
Berdon Syndrome
CTNS
Cystinosis
SRD5A2
Alopecia, Androgenetic, 1