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Diseases
Genes (320)
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MYO5B
Microvillus Inclusion Disease
TTPA
Familial Isolated Vitamin E Deficiency
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
PQBP1
Renpenning's Syndrome
IFIH1
Hepatitis E
Singleton Merten Syndrome
MC2R
Familial Glucocorticoid Deficiency
ASS1
Citrullinemia Type I
CD55
Protein Losing Enteropathy
STX3
Microvillus Inclusion Disease
RB1
Pinealoblastoma
Trilateral Retinoblastoma
MRAP
Familial Glucocorticoid Deficiency
DDX58
Hepatitis E
Singleton Merten Syndrome
CILP
Lumbar Disc Disease
COL9A3
Lumbar Disc Disease
STAR
Adrenal Crisis
Familial Glucocorticoid Deficiency
SART3
Disseminated Superficial Actinic Porokeratosis
ASPN
Lumbar Disc Disease
COL11A1
Lumbar Disc Disease
MARK3
Visual Impairment And Progressive Phthisis Bulbi
FH
Fumarase Deficiency