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Diseases
Genes (1820)
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RPS6KA3
Mental Retardation, X-Linked 23
Coffin-Lowry Syndrome
ASL
Argininosuccinic Aciduria
Necrotizing Enterocolitis
ATRX
Alpha-Thalassemia Mental Retardation Syndrome
F12
Factor Xii Deficiency
PMM2
Pmm2 Deficiency
Retinitis Pigmentosa 80
Congenital Diaphragmatic Hernia
UBE3A
Angelman Syndrome
NHS
Oculofaciocardiodental Syndrome
Nance-Horan Syndrome
SALL4
Duane-Radial Ray Syndrome
C8orf37
Retinitis Pigmentosa 80
HOXD13
Vacterl/vater Association
Vacterl Association
Congenital Diaphragmatic Hernia
PDE6B
Retinitis Pigmentosa 80
PDE6A
Retinitis Pigmentosa 80
DKC1
Dyskeratosis Congenita
TINF2
Dyskeratosis Congenita
MECP2
Alpha-Thalassemia Mental Retardation Syndrome
Mental Retardation, X-Linked 23
Angelman Syndrome
EPG5
Vici Syndrome
RHO
Optic Disc Drusen
Retinitis Pigmentosa 80
CRX
Retinitis Pigmentosa 80
RPGR
Retinitis Pigmentosa 80
RPE65
Retinitis Pigmentosa 80