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Diseases
Genes (424)
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FMR1
Disinhibition
Renpenning's Syndrome
Fragile X-Associated Tremor/ataxia Syndrome
TTPA
Familial Isolated Vitamin E Deficiency
SLC17A5
Salla Disease
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
IFIH1
Singleton Merten Syndrome
ASS1
Citrullinemia Type I
CD55
Protein Losing Enteropathy
RB1
Pinealoblastoma
Trilateral Retinoblastoma
MEN1
Gastrinoma
IL6
Fibrous Dysplasia Of Bone
Aseptic Meningitis
Familial Isolated Vitamin E Deficiency
Subacromial Bursitis
GNE
Salla Disease
DDX58
Singleton Merten Syndrome
ALB
Disinhibition
Aseptic Meningitis
Protein Losing Enteropathy
FH
Fumarase Deficiency
AKR1C3
True Hermaphroditism
AKR1C1
True Hermaphroditism
AKR1C2
True Hermaphroditism
HSD17B3
True Hermaphroditism
LHCGR
True Hermaphroditism