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: C0699739
Disease: Sensory Neuropathy, Hereditary
Sensory Neuropathy, Hereditary 		19 0 4 0.20 0 0
CUI: C1835896
Disease: SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE (disorder)
SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE (disorder) 		1 23 1 0.20 1 2.0E-02
CUI: C1840391
Disease: Pseudohypoaldosteronism, Type IIc
Pseudohypoaldosteronism, Type IIc 		1 2 1 0.20 2 7.1E-02
CUI: C1848735
Disease: Developmental delay, mild
Developmental delay, mild 		1 0 1 0.20 0 0
CUI: C1864929
Disease: Cerebellar atrophy, progressive
Cerebellar atrophy, progressive 		1 0 1 0.20 0 0
CUI: C2751092
Disease: Neuropathy, Hereditary Sensory And Autonomic, Type IIB
Neuropathy, Hereditary Sensory And Autonomic, Type IIB 		1 0 1 0.20 0 0
CUI: C3280168
Disease: NEUROPATHY, HEREDITARY SENSORY, TYPE IIC
NEUROPATHY, HEREDITARY SENSORY, TYPE IIC 		1 19 1 0.20 1 2.2E-02
CUI: C3280283
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 9
MENTAL RETARDATION, AUTOSOMAL DOMINANT 9 		1 37 1 0.20 1 1.6E-02
CUI: C4553071
Disease: Anal Pain, CTCAE 5
Anal Pain, CTCAE 5 		1 0 1 0.20 0 0
CUI: C1857171
Disease: Episodic hyperhidrosis
Episodic hyperhidrosis 		20 0 4 0.19 0 0
CUI: C0037650
Disease: Somatoform Disorder
Somatoform Disorder 		2 0 1 0.17 0 0
CUI: C0234241
Disease: Indifference to pain
Indifference to pain 		2 0 1 0.17 0 0
CUI: C1864987
Disease: Migraine, Familial Hemiplegic, 3
Migraine, Familial Hemiplegic, 3 		2 0 1 0.17 0 0
CUI: C2751756
Disease: Febrile Convulsions, Familial, 3a
Febrile Convulsions, Familial, 3a 		2 0 1 0.17 0 0
CUI: C4552061
Disease: Mandibular pain
Mandibular pain 		2 0 1 0.17 0 0
CUI: C0037140
Disease: B Virus Infection
B Virus Infection 		3 0 1 0.14 0 0
CUI: C0085649
Disease: Peripheral edema
Peripheral edema 		3 0 1 0.14 0 0
CUI: C0853946
Disease: Pain worsened
Pain worsened 		3 0 1 0.14 0 0
CUI: C3551426
Disease: Dystrophic fingernails
Dystrophic fingernails 		27 0 4 0.14 0 0
CUI: C4023408
Disease: Abnormality of mouth size
Abnormality of mouth size 		3 0 1 0.14 0 0
CUI: C1858285
Disease: Decreased number of peripheral myelinated nerve fibers
Decreased number of peripheral myelinated nerve fibers 		28 0 4 0.14 0 0
CUI: C1833661
Disease: PAROXYSMAL EXTREME PAIN DISORDER
PAROXYSMAL EXTREME PAIN DISORDER 		13 9 2 0.12 2 5.7E-02
CUI: C1858673
Disease: GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2 		4 0 1 0.12 0 0
CUI: C1855739
Disease: Indifference to Pain, Congenital, Autosomal Recessive
Indifference to Pain, Congenital, Autosomal Recessive 		23 11 3 0.12 3 8.3E-02
CUI: C0002768
Disease: Congenital Pain Insensitivity
Congenital Pain Insensitivity 		14 0 2 0.12 0 0