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Diseases
Genes (1189)
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RASA1
Sturge–weber Syndrome
Capillary Malformation-Arteriovenous Malformation
Oligodendroglioma
TYR
Albinism
Oculocutaneous Albinism Type 1a
Conjunctivitis
ABHD5
Cerebral Creatine Deficiency
HMBS
Seminoma
Acute Intermittent Porphyria
GAMT
Guanidinoacetate Methyltransferase Deficiency
GJB3
Erythrokeratodermia Variabilis Et Progressiva 3
GNAQ
Sturge–weber Syndrome
GJB4
Erythrokeratodermia Variabilis Et Progressiva 3
FGFR3
Seminoma
Syringocystadenoma Papilliferum
Pterygium Of The Conjunctiva And Cornea
IDH2
Oligodendroglioma
KIT
Phyllodes Tumor
Seminoma
Syringocystadenoma Papilliferum
TP53
Alopecia, Androgenetic, 1
Phyllodes Tumor
Seminoma
Acute Intermittent Porphyria
Pterygium Of The Conjunctiva And Cornea
Vulvar Intraepithelial Neoplasia
Oligodendroglioma
AR
Alopecia, Androgenetic, 1
Phyllodes Tumor
Seminoma
SRD5A2
Alopecia, Androgenetic, 1
BRAF
Seminoma
Syringocystadenoma Papilliferum
Oligodendroglioma
AP3D1
Albinism
MED12
Phyllodes Tumor
PSENEN
Acne Inversa, Familial, 2, With Or Without Dowling-Degos Disease
IDH1
Oligodendroglioma
HRAS
Seminoma
Syringocystadenoma Papilliferum