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Diseases
Genes (555)
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TP53
Alopecia, Androgenetic, 1
Disseminated Superficial Actinic Porokeratosis
Phyllodes Tumor
Li–fraumeni Syndrome
ABHD5
Cerebral Creatine Deficiency
MYO5B
Microvillus Inclusion Disease
GAMT
Guanidinoacetate Methyltransferase Deficiency
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
MC2R
Familial Glucocorticoid Deficiency
CHEK2
Li–fraumeni Syndrome
STX3
Microvillus Inclusion Disease
AR
Alopecia, Androgenetic, 1
Phyllodes Tumor
Li–fraumeni Syndrome
SRD5A2
Alopecia, Androgenetic, 1
MEN1
Glucagonoma
MDM2
Cerebral Creatine Deficiency
Phyllodes Tumor
Li–fraumeni Syndrome
MED12
Phyllodes Tumor
MRAP
Familial Glucocorticoid Deficiency
CDKN2A
Cerebral Creatine Deficiency
Alopecia, Androgenetic, 1
Phyllodes Tumor
Li–fraumeni Syndrome
PARP1
Alopecia, Androgenetic, 1
Meniere Disease
Salmonellosis
MTHFR
Alopecia, Androgenetic, 1
Meniere Disease
ABCC2
Alopecia, Androgenetic, 1
Salmonellosis
PRKCB
Meniere Disease
DTNA
Meniere Disease