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Diseases
Genes (598)
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ASL
Argininosuccinic Aciduria
MYO5B
Microvillus Inclusion Disease
PMM2
Pmm2 Deficiency
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
MC2R
Familial Glucocorticoid Deficiency
STX3
Microvillus Inclusion Disease
HTR2B
Valvular Heart Disease
BRAF
Erdheim–chester Disease
EPG5
Hypopigmentation
RB1
Pinealoblastoma
Trilateral Retinoblastoma
MRAP
Familial Glucocorticoid Deficiency
IL1B
Erdheim–chester Disease
Valvular Heart Disease
Leptospirosis
TNF
Hepatitis E
Social (Pragmatic) Communication Disorder
Valvular Heart Disease
Leptospirosis
Hypopigmentation
Lumbar Disc Disease
CILP
Lumbar Disc Disease
CCL2
Valvular Heart Disease
Leptospirosis
FGFR1
Valvular Heart Disease
Lumbar Disc Disease
COL9A3
Lumbar Disc Disease
SPP1
Erdheim–chester Disease
Valvular Heart Disease
IL18
Valvular Heart Disease
Leptospirosis
CASP3
Valvular Heart Disease
Leptospirosis