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: C0423122
Disease: Ptosis of eyebrow
Ptosis of eyebrow
1 0 1 0.33 0 0
CUI: C1857946
Disease: Severe gastroesophageal reflux
Severe gastroesophageal reflux
1 0 1 0.33 0 0
CUI: C1970625
Disease: Hypoplastic left atrium
Hypoplastic left atrium
1 0 1 0.33 0 0
CUI: C1970630
Disease: Agenesis of pulmonary vessels
Agenesis of pulmonary vessels
1 0 1 0.33 0 0
Cerebral Amyloid Angiopathy, Gsn-Related
1 0 1 0.33 0 0
MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 8
1 0 1 0.33 0 0
CUI: C3809803
Disease: MICROPHTHALMIA, SYNDROMIC 12
MICROPHTHALMIA, SYNDROMIC 12
1 0 1 0.33 0 0
CUI: C4021968
Disease: Aplasia/Hypoplasia of the pancreas
Aplasia/Hypoplasia of the pancreas
5 0 2 0.33 0 0
CUI: C4538849
Disease: Multilobulated spleen
Multilobulated spleen
1 0 1 0.33 0 0
Familial Amyloid Polyneuropathy, Type IV
2 0 1 0.25 0 0
CUI: C1719316
Disease: Inherited systemic amyloidosis
Inherited systemic amyloidosis
2 0 1 0.25 0 0
CUI: C1970617
Disease: Hypoplastic spleen
Hypoplastic spleen
2 0 1 0.25 0 0
CUI: C0476287
Disease: Breath-holding spell
Breath-holding spell
3 0 1 0.20 0 0
CUI: C1622345
Disease: Meretoja syndrome
Meretoja syndrome
3 0 1 0.20 0 0
CUI: C4021610
Disease: Bilateral lung agenesis
Bilateral lung agenesis
3 0 1 0.20 0 0
CUI: C4024863
Disease: Diffuse skin atrophy
Diffuse skin atrophy
3 0 1 0.20 0 0
Dermatological manifestations of systemic disorders
3 0 1 0.20 0 0
CUI: C0005742
Disease: Blepharochalasis
Blepharochalasis
4 0 1 0.17 0 0
CUI: C0242013
Disease: Sciatic Neuritis
Sciatic Neuritis
4 0 1 0.17 0 0
CUI: C0751924
Disease: Neuralgia-Neuritis, Sciatic Nerve
Neuralgia-Neuritis, Sciatic Nerve
4 0 1 0.17 0 0
CUI: C0751925
Disease: Sciatic Nerve Palsy
Sciatic Nerve Palsy
4 0 1 0.17 0 0
CUI: C1628319
Disease: Lattice corneal dystrophy Type II
Lattice corneal dystrophy Type II
4 0 1 0.17 0 0
CUI: C2939149
Disease: Amyloid of cornea
Amyloid of cornea
4 0 1 0.17 0 0
CUI: C4023402
Disease: Regional abnormality of skin
Regional abnormality of skin
4 0 1 0.17 0 0
Deficit in phonologic short-term memory
5 0 1 0.14 0 0