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: C0017671
Disease: Glomus Jugulare Tumor
Glomus Jugulare Tumor
5 0 2 0.14 0 0
CUI: C0917808
Disease: Vegetative State
Vegetative State
5 0 2 0.14 0 0
CUI: C1845245
Disease: Lower limb hypertonia
Lower limb hypertonia
21 0 4 0.14 0 0
CUI: C1859178
Disease: Progressive peripheral neuropathy
Progressive peripheral neuropathy
5 0 2 0.14 0 0
CUI: C1387805
Disease: Episodic paroxysmal anxiety
Episodic paroxysmal anxiety
14 0 3 0.14 0 0
CUI: C1868393
Disease: Elevated urinary epinephrine
Elevated urinary epinephrine
14 0 3 0.14 0 0
CUI: C0017083
Disease: Gangliosidoses
Gangliosidoses
6 0 2 0.13 0 0
CUI: C0730303
Disease: Capillary hemangioma of retina
Capillary hemangioma of retina
15 0 3 0.13 0 0
CUI: C1333993
Disease: hereditary paraganglioma
hereditary paraganglioma
15 0 3 0.13 0 0
CUI: C4022998
Disease: Arachnoid hemangiomatosis
Arachnoid hemangiomatosis
15 0 3 0.13 0 0
CUI: C4023099
Disease: Elevated urinary dopamine
Elevated urinary dopamine
15 0 3 0.13 0 0
CUI: C4025594
Disease: Positive regitine blocking test
Positive regitine blocking test
15 0 3 0.13 0 0
CUI: C4025626
Disease: Elevated urinary norepinephrine
Elevated urinary norepinephrine
15 0 3 0.13 0 0
CUI: C0007279
Disease: Carotid Body Paraganglioma
Carotid Body Paraganglioma
7 0 2 0.12 0 0
CUI: C0522357
Disease: Vertigo, Paroxysmal
Vertigo, Paroxysmal
16 0 3 0.12 0 0
MICROCEPHALY, PRIMARY AUTOSOMAL RECESSIVE, 1
7 0 2 0.12 0 0
CUI: C4293708
Disease: Recurrent paroxysmal headache
Recurrent paroxysmal headache
16 0 3 0.12 0 0
CUI: C0037899
Disease: Sphingolipidoses
Sphingolipidoses
17 0 3 0.12 0 0
CUI: C1868394
Disease: Elevated calcitonin
Elevated calcitonin
17 0 3 0.12 0 0
CUI: C0279821
Disease: metastatic pheochromocytoma
metastatic pheochromocytoma
8 0 2 0.12 0 0
Metastatic Adrenal Gland Pheochromocytoma
8 0 2 0.12 0 0
CUI: C1857175
Disease: Episodic hypertension
Episodic hypertension
8 0 2 0.12 0 0
CUI: C2237142
Disease: Moderate global developmental delay
Moderate global developmental delay
27 0 4 0.12 0 0
CUI: C4025896
Disease: Abnormality of the penis
Abnormality of the penis
8 0 2 0.12 0 0
CUI: C1849097
Disease: Loss of ability to walk
Loss of ability to walk
37 0 5 0.12 0 0