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: C0522216
Disease: Abnormal auditory evoked potential
Abnormal auditory evoked potential 		0 2 0 0 1 1.7E-02
CUI: C0917967
Disease: Pupillary Functions, Abnormal
Pupillary Functions, Abnormal 		0 1 0 0 1 1.7E-02
CUI: C1843700
Disease: Increased variability in muscle fiber diameter
Increased variability in muscle fiber diameter 		0 4 0 0 1 1.6E-02
CUI: C1857640
Disease: Decreased nerve conduction velocity
Decreased nerve conduction velocity 		0 5 0 0 1 1.6E-02
CUI: C1858719
Disease: Facial muscle weakness of muscles innervated by CN VII
Facial muscle weakness of muscles innervated by CN VII 		0 3 0 0 1 1.7E-02
CUI: C4479603
Disease: NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, NEUROPATHY, AND DEAFNESS
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, NEUROPATHY, AND DEAFNESS 		0 5 0 0 1 1.6E-02
CUI: C0020039
Disease: Hostility
Hostility 		1 0 1 2.0E-02 0 0
CUI: C0021712
Disease: Myoclonus, Intention
Myoclonus, Intention 		1 0 1 2.0E-02 0 0
CUI: C0025060
Disease: Mediastinal Cyst
Mediastinal Cyst 		1 0 1 2.0E-02 0 0
CUI: C0025467
Disease: Mesenteric Cyst
Mesenteric Cyst 		1 2 1 2.0E-02 2 3.4E-02
CUI: C0026210
Disease: Mirror Writing
Mirror Writing 		1 0 1 2.0E-02 0 0
CUI: C0030214
Disease: Myoclonus, Palatal
Myoclonus, Palatal 		1 0 1 2.0E-02 0 0
CUI: C0042907
Disease: Vitreous Detachment
Vitreous Detachment 		1 0 1 2.0E-02 0 0
CUI: C0152207
Disease: Alternating Exotropia
Alternating Exotropia 		1 1 1 2.0E-02 1 1.7E-02
CUI: C0206619
Disease: Lymphatic Vessel Tumors
Lymphatic Vessel Tumors 		1 2 1 2.0E-02 2 3.4E-02
CUI: C0220692
Disease: Maxillonasal dysplasia, Binder type
Maxillonasal dysplasia, Binder type 		1 0 1 2.0E-02 0 0
CUI: C0232180
Disease: Cardiac shunt
Cardiac shunt 		1 2 1 2.0E-02 2 3.4E-02
CUI: C0233283
Disease: Complete breech presentation
Complete breech presentation 		1 1 1 2.0E-02 1 1.7E-02
CUI: C0238525
Disease: Sarcoma of vulva
Sarcoma of vulva 		1 0 1 2.0E-02 0 0
CUI: C0239846
Disease: Hand-wringing
Hand-wringing 		1 0 1 2.0E-02 0 0
CUI: C0263421
Disease: Acrodermatitis atrophicans chronica
Acrodermatitis atrophicans chronica 		1 0 1 2.0E-02 0 0
CUI: C0265404
Disease: 4q partial monosomy syndrome
4q partial monosomy syndrome 		1 0 1 2.0E-02 0 0
CUI: C0266177
Disease: Megaduodenum
Megaduodenum 		1 0 1 2.0E-02 0 0
CUI: C0266384
Disease: Congenital absence of uterus
Congenital absence of uterus 		1 0 1 2.0E-02 0 0
CUI: C0266692
Disease: Craniopagus
Craniopagus 		1 0 1 2.0E-02 0 0