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Diseases
Genes (311)
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MYO5B
Microvillus Inclusion Disease
TTPA
Familial Isolated Vitamin E Deficiency
GNAS
Fibrous Dysplasia Of Bone
Mccune-Albright Syndrome
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
MC2R
Familial Glucocorticoid Deficiency
IFIH1
Singleton Merten Syndrome
STX3
Microvillus Inclusion Disease
CD55
Protein Losing Enteropathy
ASS1
Citrullinemia Type I
MRAP
Familial Glucocorticoid Deficiency
RB1
Pinealoblastoma
Trilateral Retinoblastoma
CILP
Lumbar Disc Disease
STAR
Adrenal Crisis
Familial Glucocorticoid Deficiency
SART3
Disseminated Superficial Actinic Porokeratosis
COL9A3
Lumbar Disc Disease
DDX58
Singleton Merten Syndrome
ASPN
Lumbar Disc Disease
MARK3
Visual Impairment And Progressive Phthisis Bulbi