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Diseases
Genes (909)
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ABHD5
Cerebral Creatine Deficiency
TTPA
Familial Isolated Vitamin E Deficiency
GAMT
Guanidinoacetate Methyltransferase Deficiency
WRN
Werner Syndrome
SLC17A5
Salla Disease
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
IFIH1
Singleton Merten Syndrome
ASS1
Citrullinemia Type I
CTNS
Cystinosis
IL6
Aseptic Meningitis
Familial Isolated Vitamin E Deficiency
Subacromial Bursitis
Diverticulitis
Bronchopulmonary Dysplasia
SRD5A2
Alopecia, Androgenetic, 1
AR
Alopecia, Androgenetic, 1
Disinhibition
PRKAR1A
Alopecia, Androgenetic, 1
Enamel-Renal Syndrome
Werner Syndrome
IL1B
Alopecia, Androgenetic, 1
Renpenning's Syndrome
Subacromial Bursitis
Bronchopulmonary Dysplasia
Werner Syndrome
Cystinosis
RB1
Pinealoblastoma
Trilateral Retinoblastoma
FAM155A
Diverticulitis
PARP1
Alopecia, Androgenetic, 1
Werner Syndrome
GNE
Salla Disease
ZFP36
Alopecia, Androgenetic, 1
Familial Isolated Vitamin E Deficiency
Vascular Tumor