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Diseases
Genes (1040)
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NPR2
Acromesomelic Dysplasia, Maroteaux Type
Acromesomelic Dysplasia, Hunter-Thompson Type
ASL
Argininosuccinic Aciduria
MYO5B
Microvillus Inclusion Disease
POLG
Balo Concentric Sclerosis
TTPA
Familial Isolated Vitamin E Deficiency
PMM2
Pmm2 Deficiency
MED12
Ventricular Septal Defect
Fg Syndrome
GDF5
Acromesomelic Dysplasia, Maroteaux Type
Acromesomelic Dysplasia, Hunter-Thompson Type
Lumbar Disc Disease
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
TAF1
Dystonia 3, Torsion, X-Linked
PRPS1
Arts Syndrome
MC2R
Familial Glucocorticoid Deficiency
INPP5E
Joubert Syndrome 31
EDN1
Nephrosis
Nephritis
ALB
Ventricular Septal Defect
Nephrosis
Vertigo, Benign Recurrent
Nephritis
CEP120
Ventricular Septal Defect
Joubert Syndrome 31
FLNA
Fg Syndrome
Intestinal Neuronal Dysplasia
ASS1
Argininosuccinic Aciduria
Citrullinemia Type I
STX3
Microvillus Inclusion Disease
GATA4
Ventricular Septal Defect