Source: ALL
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: C0003516
Disease: Aortopulmonary Septal Defect
Aortopulmonary Septal Defect 		1 0 1 3.6E-02 0 0
CUI: C0033931
Disease: Psychophysiologic Disorders
Psychophysiologic Disorders 		1 0 1 3.6E-02 0 0
CUI: C0162627
Disease: Skin Diseases, Bacterial
Skin Diseases, Bacterial 		1 0 1 3.6E-02 0 0
CUI: C0162817
Disease: Skin Diseases, Eczematous
Skin Diseases, Eczematous 		1 0 1 3.6E-02 0 0
CUI: C0221727
Disease: Pain in esophagus (finding)
Pain in esophagus (finding) 		1 0 1 3.6E-02 0 0
CUI: C0234461
Disease: aphasic
aphasic 		1 0 1 3.6E-02 0 0
CUI: C0238014
Disease: Acute cerebellar ataxia
Acute cerebellar ataxia 		1 0 1 3.6E-02 0 0
CUI: C0263224
Disease: Flexural atopic dermatitis
Flexural atopic dermatitis 		1 0 1 3.6E-02 0 0
CUI: C0263579
Disease: Pigmented hairy epidermal nevus
Pigmented hairy epidermal nevus 		1 0 1 3.6E-02 0 0
CUI: C0338900
Disease: Psychasthenic neurosis
Psychasthenic neurosis 		1 0 1 3.6E-02 0 0
CUI: C0342759
Disease: Primary lactose intolerance
Primary lactose intolerance 		1 0 1 3.6E-02 0 0
CUI: C0344183
Disease: Exercise anaphylaxis
Exercise anaphylaxis 		1 0 1 3.6E-02 0 0
CUI: C0432300
Disease: Autosomal dominant ichthyosis vulgaris
Autosomal dominant ichthyosis vulgaris 		1 0 1 3.6E-02 0 0
CUI: C0454578
Disease: Receptive aphasia (finding)
Receptive aphasia (finding) 		1 0 1 3.6E-02 0 0
CUI: C0454601
Disease: Pyramidal dysarthria
Pyramidal dysarthria 		1 0 1 3.6E-02 0 0
CUI: C0455938
Disease: Large adenoids
Large adenoids 		1 0 1 3.6E-02 0 0
CUI: C0474892
Disease: Inherited disorder of keratinization
Inherited disorder of keratinization 		1 0 1 3.6E-02 0 0
CUI: C0477360
Disease: Other dystonia
Other dystonia 		1 0 1 3.6E-02 0 0
CUI: C0542165
Disease: Pseudoparkinsonism
Pseudoparkinsonism 		1 0 1 3.6E-02 0 0
CUI: C0598121
Disease: Hypoglycorrhachia
Hypoglycorrhachia 		1 0 1 3.6E-02 0 0
CUI: C0745745
Disease: liver disease parenchymal
liver disease parenchymal 		1 0 1 3.6E-02 0 0
CUI: C0795927
Disease: Deafness, congenital onychodystrophy, recessive form
Deafness, congenital onychodystrophy, recessive form 		1 0 1 3.6E-02 0 0
CUI: C0848200
Disease: Afterbirth pain
Afterbirth pain 		1 0 1 3.6E-02 0 0
CUI: C1276070
Disease: Infantile atopic dermatitis
Infantile atopic dermatitis 		1 0 1 3.6E-02 0 0
CUI: C1304136
Disease: Onset of psoriasis in childhood (1-10 years)
Onset of psoriasis in childhood (1-10 years) 		1 0 1 3.6E-02 0 0