Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Generalized Epilepsy With Febrile Seizures Plus, 7
2 0 2 0.33 0 0
CUI: C3151229
Disease: FEBRILE SEIZURES, FAMILIAL, 3B
FEBRILE SEIZURES, FAMILIAL, 3B
2 0 2 0.33 0 0
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IID
2 0 2 0.33 0 0
CUI: C4023408
Disease: Abnormality of mouth size
Abnormality of mouth size
3 0 2 0.29 0 0
Acute episodes of neuropathic symptoms
4 3 2 0.25 1 0.20
Early Infantile Epileptic Encephalopathy 6
4 0 2 0.25 0 0
Neuropathy, Hereditary Sensory And Autonomic, Type IIA
5 0 2 0.22 0 0
CUI: C0014805
Disease: Primary Erythermalgia
Primary Erythermalgia
7 14 2 0.18 1 6.2E-02
CUI: C0234259
Disease: Sensitive to smells
Sensitive to smells
1 0 1 0.17 0 0
CUI: C0238637
Disease: Anal pain
Anal pain
1 0 1 0.17 0 0
CUI: C0240940
Disease: Scalp pain
Scalp pain
1 0 1 0.17 0 0
CUI: C0271291
Disease: Corneal anesthesia
Corneal anesthesia
1 0 1 0.17 0 0
SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder)
1 0 1 0.17 0 0
CUI: C1851697
Disease: Pancreatic islet cell adenoma
Pancreatic islet cell adenoma
1 0 1 0.17 0 0
CUI: C4017330
Disease: LIPOMA, SOMATIC
LIPOMA, SOMATIC
1 0 1 0.17 0 0
CUI: C4017331
Disease: ANGIOFIBROMA, SOMATIC
ANGIOFIBROMA, SOMATIC
1 0 1 0.17 0 0
CUI: C4017332
Disease: ADRENAL ADENOMA, SOMATIC
ADRENAL ADENOMA, SOMATIC
1 0 1 0.17 0 0
Premature eruption of permanent teeth
1 0 1 0.17 0 0
CUI: C4024855
Disease: Lack of subcutaneous fatty tissue
Lack of subcutaneous fatty tissue
1 0 1 0.17 0 0
CUI: C4225268
Disease: CUTIS LAXA, AUTOSOMAL DOMINANT 3
CUTIS LAXA, AUTOSOMAL DOMINANT 3
1 0 1 0.17 0 0
SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE
1 0 1 0.17 0 0
NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES
1 0 1 0.17 0 0
CUI: C4553071
Disease: Anal Pain, CTCAE 5
Anal Pain, CTCAE 5
1 0 1 0.17 0 0
CUI: C0037650
Disease: Somatoform Disorder
Somatoform Disorder
2 0 1 0.14 0 0
CUI: C0234241
Disease: Indifference to pain
Indifference to pain
2 0 1 0.14 0 0