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Diseases
Genes (857)
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POLG
Balo Concentric Sclerosis
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
ACTG2
Bronchopulmonary Dysplasia
Berdon Syndrome
FLNA
Intestinal Neuronal Dysplasia
Bronchopulmonary Dysplasia
Fg Syndrome
ASS1
Citrullinemia Type I
MYH11
Berdon Syndrome
MYLK
Berdon Syndrome
CTNS
Cystinosis
IL6
Aseptic Meningitis
Familial Isolated Vitamin E Deficiency
Subacromial Bursitis
Diverticulitis
Bronchopulmonary Dysplasia
IL1B
Renpenning's Syndrome
Subacromial Bursitis
Bronchopulmonary Dysplasia
Werner Syndrome
Cystinosis
FAM155A
Diverticulitis
RB1
Pinealoblastoma
Trilateral Retinoblastoma
GNE
Salla Disease