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Diseases
Genes (432)
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ABHD5
Cerebral Creatine Deficiency
MYO5B
Microvillus Inclusion Disease
GAMT
Guanidinoacetate Methyltransferase Deficiency
ACTG2
Berdon Syndrome
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
GNAS
Mccune-Albright Syndrome
TTC7A
Gastrointestinal Defects And Immunodeficiency Syndrome
MC2R
Familial Glucocorticoid Deficiency
MYH11
Berdon Syndrome
MYLK
Berdon Syndrome
STX3
Microvillus Inclusion Disease
SRD5A2
Alopecia, Androgenetic, 1
AR
Placental Site Trophoblastic Tumor
Alopecia, Androgenetic, 1
RB1
Pinealoblastoma
Trilateral Retinoblastoma
MRAP
Familial Glucocorticoid Deficiency
VDR
Alopecia, Androgenetic, 1
Lumbar Disc Disease
LMOD1
Berdon Syndrome
FLNA
Intestinal Neuronal Dysplasia
SOX10
Yemenite Deaf-Blind Hypopigmentation Syndrome
CILP
Lumbar Disc Disease