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: C2242456
Disease: thyroid function
thyroid function
7 60 2 0.18 1 1.5E-02
CUI: C0555197
Disease: Florid cemento-osseous dysplasia
Florid cemento-osseous dysplasia
1 0 1 0.17 0 0
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
1 0 1 0.17 0 0
CUI: C1997262
Disease: Hypothyroidism in pregnancy
Hypothyroidism in pregnancy
1 1 1 0.17 1 0.14
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 3
1 0 1 0.17 0 0
CUI: C3495361
Disease: Gigantiform Cementoma, Familial
Gigantiform Cementoma, Familial
1 0 1 0.17 0 0
Symmetric lesions of the basal ganglia
1 0 1 0.17 0 0
STRIATAL DEGENERATION, AUTOSOMAL DOMINANT 1
1 0 1 0.17 0 0
Thyroid stimulating hormone measurement
42 83 6 0.14 7 8.4E-02
CUI: C0240952
Disease: Dysarthria, Scanning
Dysarthria, Scanning
2 0 1 0.14 0 0
CUI: C0454597
Disease: Dysarthria, Flaccid
Dysarthria, Flaccid
2 0 1 0.14 0 0
CUI: C0454598
Disease: Dysarthria, Mixed
Dysarthria, Mixed
2 0 1 0.14 0 0
CUI: C0586738
Disease: Calf muscle weakness
Calf muscle weakness
2 0 1 0.14 0 0
CUI: C1563666
Disease: Dysarthria, Guttural
Dysarthria, Guttural
2 0 1 0.14 0 0
CUI: C1833739
Disease: Diaphyseal cortical sclerosis
Diaphyseal cortical sclerosis
2 0 1 0.14 0 0
Striatal Degeneration, Autosomal Dominant
2 0 1 0.14 0 0
CUI: C2750076
Disease: Miyoshi Muscular Dystrophy 3
Miyoshi Muscular Dystrophy 3
2 0 1 0.14 0 0
CUI: C1290708
Disease: Osteomyelitis of mandible
Osteomyelitis of mandible
3 0 1 0.12 0 0
Atrophy of quadriceps femoris muscle
3 0 1 0.12 0 0
CUI: C4025576
Disease: EMG: myotonic runs
EMG: myotonic runs
3 0 1 0.12 0 0
Internally nucleated skeletal muscle fibers
3 0 1 0.12 0 0
CUI: C0240679
Disease: Pelvic girdle muscle atrophy
Pelvic girdle muscle atrophy
4 0 1 0.11 0 0
Pigmented micronodular adrenocortical disease
4 0 1 0.11 0 0
CUI: C0231519
Disease: Gegenhalten
Gegenhalten
5 0 1 1.0E-01 0 0
CUI: C0233608
Disease: Catatonic Rigidity
Catatonic Rigidity
5 0 1 1.0E-01 0 0