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Diseases
Genes (820)
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ASL
Argininosuccinic Aciduria
COL2A1
Spondyloepiphyseal Dysplasia Congenita
TTPA
Familial Isolated Vitamin E Deficiency
SLC4A11
Corneal Dystrophy And Perceptive Deafness
Chandler's Syndrome
MYO5B
Microvillus Inclusion Disease
PMM2
Pmm2 Deficiency
LIM2
Cataract 19, Multiple Types
IFIH1
Singleton Merten Syndrome
STX3
Microvillus Inclusion Disease
CCL2
Asthma Attack
Bronchial Hyperresponsiveness
NR3C1
Hypoglycemia
High-Altitude Pulmonary Edema
Obstructive Lung Disease
PTEN
Anisometropia
Hypoglycemia
Lumbar Disc Disease
RB1
Pinealoblastoma
Hypoglycemia
Trilateral Retinoblastoma
ADAM33
Asthma Attack
Bronchial Hyperresponsiveness
ABCC8
Hypoglycemia
IGF2
Hypoglycemia
SERAC1
Hypoglycemia
CCNO
Obstructive Lung Disease
TNF
Asthma Attack
Hypoglycemia
Obstructive Lung Disease
Lumbar Disc Disease
Familial Isolated Vitamin E Deficiency
Bronchial Hyperresponsiveness
IL13
Asthma Attack
Bronchial Hyperresponsiveness