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: C0281913
Disease: Swelling of skeletal muscle
Swelling of skeletal muscle
2 0 2 8.0E-02 0 0
CUI: C1847827
Disease: LIG4 Syndrome
LIG4 Syndrome
2 13 2 8.0E-02 1 4.8E-02
CUI: C1849779
Disease: Kowarski syndrome
Kowarski syndrome
2 0 2 8.0E-02 0 0
Specific disorders of sleep of non-organic origin
3 0 2 7.7E-02 0 0
Isolated Growth Hormone Deficiency, Type II
3 0 2 7.7E-02 0 0
CUI: C1868578
Disease: Patellar aplasia
Patellar aplasia
17 0 3 7.7E-02 0 0
CUI: C0014008
Disease: Empty Sella Syndrome
Empty Sella Syndrome
4 0 2 7.4E-02 0 0
CUI: C0271695
Disease: Rabson-Mendenhall Syndrome
Rabson-Mendenhall Syndrome
4 0 2 7.4E-02 0 0
CUI: C0340987
Disease: Splenic atrophy
Splenic atrophy
4 0 2 7.4E-02 0 0
CUI: C1840069
Disease: Sandal gap
Sandal gap
62 0 6 7.4E-02 0 0
Growth Hormone Insensitivity Syndrome
4 0 2 7.4E-02 0 0
CUI: C1857665
Disease: Aplastic clavicle
Aplastic clavicle
19 0 3 7.3E-02 0 0
CUI: C4551705
Disease: Abnormality of chromosome stability
Abnormality of chromosome stability
34 0 4 7.3E-02 0 0
CUI: C0241703
Disease: High pitched voice
High pitched voice
35 0 4 7.1E-02 0 0
CUI: C0265205
Disease: Robinow Syndrome
Robinow Syndrome
20 0 3 7.1E-02 0 0
CUI: C0271568
Disease: Laron Syndrome
Laron Syndrome
20 0 3 7.1E-02 0 0
CUI: C0405578
Disease: Gigantism and acromegaly
Gigantism and acromegaly
5 0 2 7.1E-02 0 0
CUI: C0744483
Disease: growth hormone treatment
growth hormone treatment
20 0 3 7.1E-02 0 0
CUI: C0858734
Disease: Insulin hypoglycemia
Insulin hypoglycemia
5 0 2 7.1E-02 0 0
CUI: C1849524
Disease: Pygmy (disorder)
Pygmy (disorder)
5 0 2 7.1E-02 0 0
CUI: C1860105
Disease: Severe short-limb dwarfism
Severe short-limb dwarfism
5 0 2 7.1E-02 0 0
CUI: C0740749
Disease: Chronic metabolic acidosis
Chronic metabolic acidosis
6 0 2 6.9E-02 0 0
CUI: C1971021
Disease: Potassium depletion
Potassium depletion
6 0 2 6.9E-02 0 0
CUI: C0238402
Disease: Pycnodysostosis
Pycnodysostosis
7 0 2 6.7E-02 0 0
CUI: C1956147
Disease: Microlissencephaly
Microlissencephaly
40 0 4 6.6E-02 0 0