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Diseases
Genes (354)
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MYO5B
Microvillus Inclusion Disease
TTPA
Familial Isolated Vitamin E Deficiency
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
ABCC9
Cantú Syndrome
PQBP1
Renpenning's Syndrome
PITX3
Anterior Segment Dysgenesis 1
MC2R
Familial Glucocorticoid Deficiency
IFIH1
Singleton Merten Syndrome
KCNJ8
Cantú Syndrome
LIPA
Acid Lipase Disease
FOXE3
Anterior Segment Dysgenesis 1
STX3
Microvillus Inclusion Disease
CD55
Protein Losing Enteropathy
PXDN
Anterior Segment Dysgenesis 1
RB1
Pinealoblastoma
Trilateral Retinoblastoma
MRAP
Familial Glucocorticoid Deficiency
MEN1
Gastrinoma
CILP
Lumbar Disc Disease
STAR
Adrenal Crisis
Familial Glucocorticoid Deficiency
COL9A3
Lumbar Disc Disease