Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Pleural Epithelioid Hemangioendothelioma
1 0 1 1.00 0 0
CUI: C0561843
Disease: Memory, Episodic
Memory, Episodic
2 0 1 0.50 0 0
CUI: C3551041
Disease: Short ear
Short ear
2 0 1 0.50 0 0
Liver Epithelioid Hemangioendothelioma
3 0 1 0.33 0 0
CUI: C0266030
Disease: Supernumerary mesiodens tooth
Supernumerary mesiodens tooth
5 0 1 0.20 0 0
CUI: C4476644
Disease: Segmental myoclonic seizures
Segmental myoclonic seizures
5 0 1 0.20 0 0
CUI: C1848453
Disease: Poor motor coordination
Poor motor coordination
6 0 1 0.17 0 0
CUI: C4476822
Disease: Hypoplastic hippocampus
Hypoplastic hippocampus
7 0 1 0.14 0 0
Cutaneous Fibrous Histiocytoma, Epithelioid Variant
8 0 1 0.12 0 0
CUI: C1845029
Disease: Nonprogressive cerebellar ataxia
Nonprogressive cerebellar ataxia
9 0 1 0.11 0 0
CUI: C0345907
Disease: Angiosarcoma of liver
Angiosarcoma of liver
11 0 1 9.1E-02 0 0
CUI: C4315130
Disease: Hippocampal atrophy
Hippocampal atrophy
13 0 1 7.7E-02 0 0
CUI: C0742034
Disease: cerebellar function
cerebellar function
14 0 1 7.1E-02 0 0
CUI: C1839783
Disease: Large forehead
Large forehead
14 0 1 7.1E-02 0 0
CUI: C1856019
Disease: Abnormal cortical gyration
Abnormal cortical gyration
17 0 1 5.9E-02 0 0
CUI: C4021087
Disease: Abnormal social behavior
Abnormal social behavior
19 0 1 5.3E-02 0 0
CUI: C0162285
Disease: Edema of eyelid
Edema of eyelid
22 0 1 4.5E-02 0 0
CUI: C0018915
Disease: Hemangioendothelioma
Hemangioendothelioma
26 0 1 3.8E-02 0 0
Autosomal dominant compelling helio ophthalmic outburst syndrome
26 0 1 3.8E-02 0 0
Childhood Epithelioid Hemangioendothelioma
26 0 1 3.8E-02 0 0
Adult Epithelioid Hemangioendothelioma
26 0 1 3.8E-02 0 0
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
27 0 1 3.7E-02 0 0
Epithelioid hemangioendothelioma, malignant
29 0 1 3.4E-02 0 0
CUI: C2673700
Disease: Brisk reflexes
Brisk reflexes
31 0 1 3.2E-02 0 0
AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE
31 0 1 3.2E-02 0 0