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: C0235910
Disease: Colagenosis
Colagenosis
1 0 1 1.00 0 0
Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Unusual Plaques
1 0 1 1.00 0 0
CUI: C3151038
Disease: ACNE INVERSA, FAMILIAL, 3
ACNE INVERSA, FAMILIAL, 3
1 0 1 1.00 0 0
CUI: C3160720
Disease: Cardiomyopathy, Dilated, 1u
Cardiomyopathy, Dilated, 1u
1 0 1 1.00 0 0
ALZHEIMER DISEASE, FAMILIAL, WITH SPASTIC PARAPARESIS AND UNUSUAL PLAQUES
1 0 1 1.00 0 0
ALZHEIMER DISEASE, FAMILIAL, 3, WITH UNUSUAL PLAQUES
1 0 1 1.00 0 0
ALZHEIMER DISEASE, FAMILIAL, 3, WITH SPASTIC PARAPARESIS
1 0 1 1.00 0 0
CUI: C4022899
Disease: Bilateral wrist flexion contracture
Bilateral wrist flexion contracture
1 0 1 1.00 0 0
CUI: C4703584
Disease: Optic ataxia
Optic ataxia
1 0 1 1.00 0 0
CUI: C0234512
Disease: Prosopagnosia
Prosopagnosia
2 0 1 0.50 0 0
CUI: C0263006
Disease: Perifolliculitis
Perifolliculitis
2 0 1 0.50 0 0
CUI: C0474420
Disease: Inappropriate sexual behavior
Inappropriate sexual behavior
3 0 1 0.33 0 0
CUI: C4022574
Disease: Limb apraxia
Limb apraxia
3 1 1 0.33 1 0.50
CUI: C4024935
Disease: Subcortical dementia
Subcortical dementia
3 0 1 0.33 0 0
CUI: C4023521
Disease: Chronic furunculosis
Chronic furunculosis
4 0 1 0.25 0 0
CUI: C4477086
Disease: Cotton wool plaques
Cotton wool plaques
4 0 1 0.25 0 0
CUI: C0409336
Disease: Flexion contracture-shoulder
Flexion contracture-shoulder
5 0 1 0.20 0 0
CUI: C0701811
Disease: Poor short-term memory
Poor short-term memory
5 0 1 0.20 0 0
CUI: C0917814
Disease: Aphasia, Expressive
Aphasia, Expressive
5 0 1 0.20 0 0
CUI: C1840560
Disease: Hidradenitis suppurativa, familial
Hidradenitis suppurativa, familial
5 0 1 0.20 0 0
CUI: C2676500
Disease: COWDEN-LIKE SYNDROME (disorder)
COWDEN-LIKE SYNDROME (disorder)
5 0 1 0.20 0 0
CUI: C3840049
Disease: Dysexecutive syndrome
Dysexecutive syndrome
5 0 1 0.20 0 0
Sporadic Cerebral Amyloid Angiopathy
6 0 1 0.17 0 0
CUI: C1853766
Disease: Pontocerebellar atrophy
Pontocerebellar atrophy
6 0 1 0.17 0 0
CUI: C2677567
Disease: DYSTONIA 16 (disorder)
DYSTONIA 16 (disorder)
6 0 1 0.17 0 0