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: C0003028
Disease: Anhidrosis
Anhidrosis 		37 0 6 0.15 0 0
CUI: C1855739
Disease: Indifference to Pain, Congenital, Autosomal Recessive
Indifference to Pain, Congenital, Autosomal Recessive 		23 0 4 0.15 0 0
CUI: C4021222
Disease: Impaired temperature sensation
Impaired temperature sensation 		8 0 2 0.14 0 0
CUI: C3551426
Disease: Dystrophic fingernails
Dystrophic fingernails 		27 0 4 0.13 0 0
CUI: C0025164
Disease: Megaesophagus
Megaesophagus 		10 0 2 0.12 0 0
CUI: C0234229
Disease: Deep pain
Deep pain 		1 0 1 0.12 0 0
CUI: C0234259
Disease: Sensitive to smells
Sensitive to smells 		1 0 1 0.12 0 0
CUI: C0238637
Disease: Anal pain
Anal pain 		1 0 1 0.12 0 0
CUI: C0240940
Disease: Scalp pain
Scalp pain 		1 0 1 0.12 0 0
CUI: C0271291
Disease: Corneal anesthesia
Corneal anesthesia 		1 0 1 0.12 0 0
CUI: C0346363
Disease: Nevus of conjunctiva
Nevus of conjunctiva 		1 0 1 0.12 0 0
CUI: C0403639
Disease: Chemical cystitis
Chemical cystitis 		1 0 1 0.12 0 0
CUI: C1319183
Disease: Corticosteroid induced cataract
Corticosteroid induced cataract 		1 0 1 0.12 0 0
CUI: C1697976
Disease: Hypotestosteronism
Hypotestosteronism 		1 0 1 0.12 0 0
CUI: C1835896
Disease: SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE (disorder)
SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE (disorder) 		1 0 1 0.12 0 0
CUI: C1840391
Disease: Pseudohypoaldosteronism, Type IIc
Pseudohypoaldosteronism, Type IIc 		1 0 1 0.12 0 0
CUI: C1848735
Disease: Developmental delay, mild
Developmental delay, mild 		1 0 1 0.12 0 0
CUI: C1850407
Disease: Navajo Familial Neurogenic Arthropathy
Navajo Familial Neurogenic Arthropathy 		1 0 1 0.12 0 0
CUI: C1864929
Disease: Cerebellar atrophy, progressive
Cerebellar atrophy, progressive 		1 0 1 0.12 0 0
CUI: C2751092
Disease: Neuropathy, Hereditary Sensory And Autonomic, Type IIB
Neuropathy, Hereditary Sensory And Autonomic, Type IIB 		1 0 1 0.12 0 0
CUI: C3280168
Disease: NEUROPATHY, HEREDITARY SENSORY, TYPE IIC
NEUROPATHY, HEREDITARY SENSORY, TYPE IIC 		1 0 1 0.12 0 0
CUI: C3280283
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 9
MENTAL RETARDATION, AUTOSOMAL DOMINANT 9 		1 0 1 0.12 0 0
CUI: C3854438
Disease: Rapidly progressive osteoarthritis
Rapidly progressive osteoarthritis 		1 0 1 0.12 0 0
CUI: C4538468
Disease: MARSILI SYNDROME
MARSILI SYNDROME 		1 0 1 0.12 0 0
CUI: C4553071
Disease: Anal Pain, CTCAE 5
Anal Pain, CTCAE 5 		1 0 1 0.12 0 0