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Diseases
Genes (652)
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OPN1LW
Colorblindness, Partial, Protan Series
Color Blindness
Color Vision Deficiency
OPN1MW
Colorblindness, Partial, Deutan Series
Color Vision Deficiency
ABHD5
Cerebral Creatine Deficiency
MYO5B
Microvillus Inclusion Disease
ATRX
Alpha-Thalassemia Mental Retardation Syndrome
GAMT
Guanidinoacetate Methyltransferase Deficiency
BEST1
Vitelliform Macular Dystrophy
MED12
Fg Syndrome
Alpha-Thalassemia Mental Retardation Syndrome
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
UBA1
X-Linked Spinal Muscular Atrophy Type 2
MC2R
Familial Glucocorticoid Deficiency
NR2E3
Color Vision Deficiency
Goldmann-Favre Syndrome
BLVRA
Hyperbiliverdinemia
OFD1
Orofaciodigital Syndrome 1
STX3
Microvillus Inclusion Disease
SRD5A2
Alopecia, Androgenetic, 1
AR
Alopecia, Androgenetic, 1
Colorblindness, Partial, Protan Series
TMEM107
Orofaciodigital Syndrome 1
CNGA3
Color Blindness
Color Vision Deficiency
PRPH2
Vitelliform Macular Dystrophy