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: C0016512
Disease: Foot pain
Foot pain 		1 0 1 3.1E-02 0 0
CUI: C0029897
Disease: Otorhinolaryngologic Neoplasms
Otorhinolaryngologic Neoplasms 		1 0 1 3.1E-02 0 0
CUI: C0042850
Disease: Vitamin B Deficiency
Vitamin B Deficiency 		1 0 1 3.1E-02 0 0
CUI: C0234229
Disease: Deep pain
Deep pain 		1 0 1 3.1E-02 0 0
CUI: C0270804
Disease: Spastic Diplegia Cerebral Palsy
Spastic Diplegia Cerebral Palsy 		1 0 1 3.1E-02 0 0
CUI: C0302883
Disease: SMITH DISEASE
SMITH DISEASE 		1 0 1 3.1E-02 0 0
CUI: C0345982
Disease: Multiple self-healing epithelioma of Ferguson-Smith
Multiple self-healing epithelioma of Ferguson-Smith 		1 0 1 3.1E-02 0 0
CUI: C0346363
Disease: Nevus of conjunctiva
Nevus of conjunctiva 		1 0 1 3.1E-02 0 0
CUI: C0403639
Disease: Chemical cystitis
Chemical cystitis 		1 0 1 3.1E-02 0 0
CUI: C0740487
Disease: Maxillary Sinus Carcinoma
Maxillary Sinus Carcinoma 		1 0 1 3.1E-02 0 0
CUI: C0751761
Disease: Upper Airway Resistance Sleep Apnea Syndrome
Upper Airway Resistance Sleep Apnea Syndrome 		1 0 1 3.1E-02 0 0
CUI: C1319183
Disease: Corticosteroid induced cataract
Corticosteroid induced cataract 		1 0 1 3.1E-02 0 0
CUI: C1504369
Disease: Allergic disorder of respiratory system
Allergic disorder of respiratory system 		1 0 1 3.1E-02 0 0
CUI: C1697976
Disease: Hypotestosteronism
Hypotestosteronism 		1 0 1 3.1E-02 0 0
CUI: C1708341
Disease: Heavier Menses
Heavier Menses 		1 0 1 3.1E-02 0 0
CUI: C1836485
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2 (disorder)
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2 (disorder) 		1 0 1 3.1E-02 0 0
CUI: C1858804
Disease: Cerebellar Ataxia, Deafness, and Narcolepsy
Cerebellar Ataxia, Deafness, and Narcolepsy 		1 0 1 3.1E-02 0 0
CUI: C1861678
Disease: Charcot-Marie-Tooth Disease, Axonal, Type 2a1
Charcot-Marie-Tooth Disease, Axonal, Type 2a1 		1 0 1 3.1E-02 0 0
CUI: C2751092
Disease: Neuropathy, Hereditary Sensory And Autonomic, Type IIB
Neuropathy, Hereditary Sensory And Autonomic, Type IIB 		1 0 1 3.1E-02 0 0
CUI: C3150896
Disease: NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC 		1 5 1 3.1E-02 1 5.6E-02
CUI: C3150972
Disease: NEUROPATHY, HEREDITARY SENSORY, TYPE ID
NEUROPATHY, HEREDITARY SENSORY, TYPE ID 		1 0 1 3.1E-02 0 0
CUI: C3279885
Disease: Hereditary Sensory and Autonomic Neuropathy Type Ie
Hereditary Sensory and Autonomic Neuropathy Type Ie 		1 0 1 3.1E-02 0 0
CUI: C3810194
Disease: NEUROPATHY, HEREDITARY SENSORY, TYPE IF
NEUROPATHY, HEREDITARY SENSORY, TYPE IF 		1 1 1 3.1E-02 1 7.1E-02
CUI: C3854438
Disease: Rapidly progressive osteoarthritis
Rapidly progressive osteoarthritis 		1 0 1 3.1E-02 0 0
CUI: C4016942
Disease: NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE 		1 1 1 3.1E-02 1 7.1E-02