Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C1847507
Disease: Paroxysmal lethargy
Paroxysmal lethargy
1 0 1 0.25 0 0
POLYOSTOTIC FIBROUS DYSPLASIA, SOMATIC, MOSAIC
1 0 1 0.25 0 0
CUI: C2936444
Disease: Pyogenic Sacroiliitis
Pyogenic Sacroiliitis
1 0 1 0.25 0 0
CUI: C2936445
Disease: Septic Sacroiliitis
Septic Sacroiliitis
1 0 1 0.25 0 0
CUI: C2937224
Disease: Constitutional obesity
Constitutional obesity
6 0 2 0.25 0 0
GLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE
1 0 1 0.25 0 0
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 12
1 0 1 0.25 0 0
CUI: C3888993
Disease: Hypocortisolaemia
Hypocortisolaemia
1 0 1 0.25 0 0
PSEUDOHYPOPARATHYROIDISM, TYPE IA, WITH TESTOTOXICOSIS
1 0 1 0.25 0 0
OBESITY, EARLY-ONSET, SUSCEPTIBILITY TO
1 0 1 0.25 0 0
CUI: C4024097
Disease: Broad 1st metacarpal
Broad 1st metacarpal
1 0 1 0.25 0 0
CUI: C4087197
Disease: Ectopic posterior pituitary gland
Ectopic posterior pituitary gland
1 0 1 0.25 0 0
CUI: C4540135
Disease: PITUITARY ADENOMA 3, MULTIPLE TYPES
PITUITARY ADENOMA 3, MULTIPLE TYPES
1 0 1 0.25 0 0
PITUITARY TUMOR 3, GROWTH HORMONE-SECRETING, SOMATIC
1 0 1 0.25 0 0
CUI: C4551966
Disease: GLUT1 DEFICIENCY SYNDROME 1
GLUT1 DEFICIENCY SYNDROME 1
1 0 1 0.25 0 0
CUI: C4727593
Disease: Crooke Cell Adenoma
Crooke Cell Adenoma
1 0 1 0.25 0 0
CUI: C0006905
Disease: Capillary Fragility
Capillary Fragility
2 0 1 0.20 0 0
CUI: C0019937
Disease: Horner Syndrome
Horner Syndrome
2 0 1 0.20 0 0
CUI: C0221436
Disease: Melanoderma (disorder)
Melanoderma (disorder)
2 0 1 0.20 0 0
Pseudohypoparathyroidism and pseudopseudohypoparathyroidism
2 0 1 0.20 0 0
CUI: C0342496
Disease: Micronodular adrenal hyperplasia
Micronodular adrenal hyperplasia
2 0 1 0.20 0 0
CUI: C0346416
Disease: Benign neuroendocrine tumor
Benign neuroendocrine tumor
2 0 1 0.20 0 0
CUI: C0391870
Disease: Abnormality of red blood cells
Abnormality of red blood cells
2 0 1 0.20 0 0
CUI: C0549609
Disease: Dysfunction adrenal
Dysfunction adrenal
2 0 1 0.20 0 0
CUI: C0553767
Disease: Congenital Cerebral Palsy
Congenital Cerebral Palsy
2 0 1 0.20 0 0