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Diseases
Genes (715)
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ABHD5
Cerebral Creatine Deficiency
MYO5B
Microvillus Inclusion Disease
GAMT
Guanidinoacetate Methyltransferase Deficiency
COL2A1
Collagen, Type Ii, Alpha-1
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
ALK
Inflammatory Myofibroblastic Tumour
MC2R
Familial Glucocorticoid Deficiency
RANBP2
Cholera
Inflammatory Myofibroblastic Tumour
Hypopigmentation
RHOA
Alopecia, Androgenetic, 1
Hypopigmentation
STX3
Microvillus Inclusion Disease
HTR2B
Valvular Heart Disease
SRD5A2
Alopecia, Androgenetic, 1
AR
Alopecia, Androgenetic, 1
EPG5
Hypopigmentation
MRAP
Familial Glucocorticoid Deficiency
TPM3
Inflammatory Myofibroblastic Tumour
IL1B
Cholera
Alopecia, Androgenetic, 1
Valvular Heart Disease
CLTC
Inflammatory Myofibroblastic Tumour
TPM4
Inflammatory Myofibroblastic Tumour
PYCARD
Cholera
Valvular Heart Disease