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Diseases
Genes (777)
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BMPR1A
Protein Losing Enteropathy
Juvenile Polyposis Syndrome
SLC6A19
Hartnup Disease
MYO5B
Microvillus Inclusion Disease
POLG
Balo Concentric Sclerosis
TTPA
Familial Isolated Vitamin E Deficiency
SMAD4
Juvenile Polyposis Syndrome
OPA3
Costeff Syndrome
SLC17A5
Salla Disease
FECH
Erythropoietic Protoporphyria
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
UMOD
Medullary Cystic Kidney Disease
MED12
Fg Syndrome
ENG
Foix-Alajouanine Syndrome
Bronchopulmonary Dysplasia
Juvenile Polyposis Syndrome
MC2R
Familial Glucocorticoid Deficiency
FLNA
Intestinal Neuronal Dysplasia
Bronchopulmonary Dysplasia
Fg Syndrome
ASS1
Citrullinemia Type I
STX3
Microvillus Inclusion Disease
CD55
Protein Losing Enteropathy
CTNS
Cystinosis
PTEN
Protein Losing Enteropathy
Juvenile Polyposis Syndrome