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: C0741146
Disease: anxiety acute
anxiety acute 		1 0 1 1.00 0 0
CUI: C0596848
Disease: lipoprotein disorder
lipoprotein disorder 		3 0 1 0.33 0 0
CUI: C1845987
Disease: Neutropenia, Severe Congenital, X-Linked
Neutropenia, Severe Congenital, X-Linked 		4 0 1 0.25 0 0
CUI: C0277873
Disease: Nasal Flaring
Nasal Flaring 		5 0 1 0.20 0 0
CUI: C1835801
Disease: Eversion of lateral third of lower eyelids
Eversion of lateral third of lower eyelids 		6 0 1 0.17 0 0
CUI: C4551517
Disease: Flared nostrils abnormality
Flared nostrils abnormality 		6 0 1 0.17 0 0
CUI: C1337012
Disease: Well-differentiated papillary mesothelioma
Well-differentiated papillary mesothelioma 		9 0 1 0.11 0 0
CUI: C1096367
Disease: Increased mean platelet volume
Increased mean platelet volume 		10 0 1 1.0E-01 0 0
CUI: C1519787
Disease: Undifferentiated Neuroblastoma
Undifferentiated Neuroblastoma 		12 0 1 8.3E-02 0 0
CUI: C4021866
Disease: obsolete Abnormal heart morphology
obsolete Abnormal heart morphology 		12 0 1 8.3E-02 0 0
CUI: C0334246
Disease: Squamous cell carcinoma, metastatic
Squamous cell carcinoma, metastatic 		13 0 1 7.7E-02 0 0
CUI: C1412000
Disease: Mesenteric vascular insufficiency
Mesenteric vascular insufficiency 		13 0 1 7.7E-02 0 0
CUI: C4551482
Disease: Adams-Oliver syndrome 1
Adams-Oliver syndrome 1 		17 0 1 5.9E-02 0 0
CUI: C4289709
Disease: DOCK8 Deficiency
DOCK8 Deficiency 		18 0 1 5.6E-02 0 0
CUI: C0341306
Disease: Microvillus inclusion disease
Microvillus inclusion disease 		19 0 1 5.3E-02 0 0
CUI: C0750887
Disease: Adrenal Cancer
Adrenal Cancer 		20 0 1 5.0E-02 0 0
CUI: C0028866
Disease: Oculomotor Nerve Paralysis
Oculomotor Nerve Paralysis 		22 0 1 4.5E-02 0 0
CUI: C0272139
Disease: Erythrocytosis due to low atmospheric pressure
Erythrocytosis due to low atmospheric pressure 		25 0 1 4.0E-02 0 0
CUI: C0282606
Disease: Myomatous neoplasm
Myomatous neoplasm 		25 0 1 4.0E-02 0 0
CUI: C3539920
Disease: ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE
ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE 		25 0 1 4.0E-02 0 0
CUI: C3887494
Disease: ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE
ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE 		25 0 1 4.0E-02 0 0
CUI: C0043046
Disease: Wasting Syndrome
Wasting Syndrome 		26 0 1 3.8E-02 0 0
CUI: C0600452
Disease: Hepatopulmonary Syndrome
Hepatopulmonary Syndrome 		29 0 1 3.4E-02 0 0
CUI: C3809250
Disease: ESTROGEN RESISTANCE
ESTROGEN RESISTANCE 		30 0 1 3.3E-02 0 0
CUI: C0039292
Disease: Tangier Disease
Tangier Disease 		31 0 1 3.2E-02 0 0