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Diseases
Genes (357)
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SMAD4
Juvenile Polyposis Syndrome
Lumbar Disc Disease
ASL
Argininosuccinic Aciduria
BMPR1A
Juvenile Polyposis Syndrome
MYO5B
Microvillus Inclusion Disease
TTPA
Familial Isolated Vitamin E Deficiency
PMM2
Pmm2 Deficiency
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
GNAS
Mccune-Albright Syndrome
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
ENG
Foix-Alajouanine Syndrome
Juvenile Polyposis Syndrome
MC2R
Familial Glucocorticoid Deficiency
IFIH1
Singleton Merten Syndrome
ASS1
Argininosuccinic Aciduria
Citrullinemia Type I
STX3
Microvillus Inclusion Disease
PTEN
Juvenile Polyposis Syndrome
Lumbar Disc Disease
RB1
Pinealoblastoma
Trilateral Retinoblastoma
MRAP
Familial Glucocorticoid Deficiency
CILP
Lumbar Disc Disease
COL9A3
Lumbar Disc Disease