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Diseases
Genes (843)
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PMM2
Pmm2 Deficiency
ASL
Argininosuccinic Aciduria
TTPA
Familial Isolated Vitamin E Deficiency
WRN
Werner Syndrome
SLC17A5
Salla Disease
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
FLNA
Intestinal Neuronal Dysplasia
Bronchopulmonary Dysplasia
Fg Syndrome
ASS1
Argininosuccinic Aciduria
Citrullinemia Type I
CTNS
Cystinosis
IL6
Argininosuccinic Aciduria
Aseptic Meningitis
Familial Isolated Vitamin E Deficiency
Subacromial Bursitis
Diverticulitis
Bronchopulmonary Dysplasia
IL1B
Renpenning's Syndrome
Subacromial Bursitis
Bronchopulmonary Dysplasia
Werner Syndrome
Cystinosis
RB1
Pinealoblastoma
Trilateral Retinoblastoma
FAM155A
Diverticulitis
GNE
Salla Disease
DDX58
Singleton Merten Syndrome
ALB
Disinhibition
Aseptic Meningitis
Bronchopulmonary Dysplasia