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Diseases
Genes (2554)
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TP53
Trichothiodystrophy
Bloom Syndrome
Werner Syndrome
Chronic Obstructive Pulmonary Disease
Li–fraumeni Syndrome
Cockayne Syndrome
Pectus Excavatum
Myotonic Dystrophy
Dyskeratosis Congenita
Retinal Detachment
WRN
Bloom Syndrome
Werner Syndrome
Cockayne Syndrome
BLM
Bloom Syndrome
Werner Syndrome
Cockayne Syndrome
ERCC2
Trichothiodystrophy
Cockayne Syndrome
TNF
Latent Tuberculosis
Bloom Syndrome
Chronic Obstructive Pulmonary Disease
Baller–gerold Syndrome
Myotonic Dystrophy
Valvular Heart Disease
Retinal Detachment
DKC1
Werner Syndrome
Hypospadias
Dyskeratosis Congenita
MMP1
Trichothiodystrophy
Chronic Obstructive Pulmonary Disease
ERCC6
Trichothiodystrophy
Cockayne Syndrome
SIX1
Branchio-Oto-Renal Syndrome
RECQL4
Bloom Syndrome
Werner Syndrome
Li–fraumeni Syndrome
Baller–gerold Syndrome
TINF2
Dyskeratosis Congenita
CASP3
Bloom Syndrome
Chronic Obstructive Pulmonary Disease
Valvular Heart Disease
Retinal Detachment
EYA1
Hypospadias
Cockayne Syndrome
Pectus Excavatum
Branchio-Oto-Renal Syndrome
ERCC8
Cockayne Syndrome
AAAS
Triple-A Syndrome
ERCC3
Trichothiodystrophy
Cockayne Syndrome
CHEK2
Bloom Syndrome
Li–fraumeni Syndrome
PDGFRB
Chronic Obstructive Pulmonary Disease
Primary Familial Brain Calcification
SLC20A2
Primary Familial Brain Calcification
SFTPD
Chronic Obstructive Pulmonary Disease