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: C0040416
Disease: Tonic Pupil
Tonic Pupil 		1 0 1 0.14 0 0
CUI: C0272405
Disease: Functional asplenia
Functional asplenia 		1 0 1 0.14 0 0
CUI: C0850629
Disease: radiating back pain
radiating back pain 		1 0 1 0.14 0 0
CUI: C1832168
Disease: BLOOD GROUP--FROESE
BLOOD GROUP--FROESE 		1 0 1 0.14 0 0
CUI: C1843075
Disease: Charcot-Marie-Tooth Disease, Dominant Intermediate D
Charcot-Marie-Tooth Disease, Dominant Intermediate D 		1 6 1 0.14 1 0.14
CUI: C1843153
Disease: Charcot-Marie-Tooth disease, Type 2J
Charcot-Marie-Tooth disease, Type 2J 		1 7 1 0.14 1 0.12
CUI: C1862190
Disease: BLOOD GROUP--WRIGHT ANTIGEN
BLOOD GROUP--WRIGHT ANTIGEN 		1 0 1 0.14 0 0
CUI: C1862191
Disease: BLOOD GROUP--WALDNER TYPE
BLOOD GROUP--WALDNER TYPE 		1 0 1 0.14 0 0
CUI: C1969039
Disease: Renal Tubular Acidosis, Distal, With Normal Red Cell Morphology
Renal Tubular Acidosis, Distal, With Normal Red Cell Morphology 		1 0 1 0.14 0 0
CUI: C2675212
Disease: Spherocytosis, Type 4
Spherocytosis, Type 4 		1 0 1 0.14 0 0
CUI: C4015898
Disease: RENAL TUBULAR ACIDOSIS, AUTOSOMAL DOMINANT
RENAL TUBULAR ACIDOSIS, AUTOSOMAL DOMINANT 		1 0 1 0.14 0 0
CUI: C4015903
Disease: SWANN BLOOD GROUP ANTIGEN PHENOTYPE
SWANN BLOOD GROUP ANTIGEN PHENOTYPE 		1 0 1 0.14 0 0
CUI: C4015904
Disease: ACANTHOCYTOSIS DUE TO BAND 3 HT
ACANTHOCYTOSIS DUE TO BAND 3 HT 		1 0 1 0.14 0 0
CUI: C4016266
Disease: CHARCOT-MARIE-TOOTH DISEASE, TYPE 1B, WITH FOCALLY FOLDED MYELIN SHEATHS
CHARCOT-MARIE-TOOTH DISEASE, TYPE 1B, WITH FOCALLY FOLDED MYELIN SHEATHS 		1 0 1 0.14 0 0
CUI: C4022665
Disease: Isothenuria
Isothenuria 		1 0 1 0.14 0 0
CUI: C4755257
Disease: Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain
Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain 		1 0 1 0.14 0 0
CUI: C0156847
Disease: Anaemia, postpartum
Anaemia, postpartum 		2 0 1 0.12 0 0
CUI: C0272051
Disease: Xerocytosis
Xerocytosis 		20 0 3 0.12 0 0
CUI: C0474520
Disease: Myokymia, Generalized
Myokymia, Generalized 		2 0 1 0.12 0 0
CUI: C0920187
Disease: Congenital neuropathy
Congenital neuropathy 		2 0 1 0.12 0 0
CUI: C1835671
Disease: Keratoderma palmoplantar spastic paralysis
Keratoderma palmoplantar spastic paralysis 		2 0 1 0.12 0 0
CUI: C1861675
Disease: Cold-induced muscle cramps
Cold-induced muscle cramps 		2 0 1 0.12 0 0
CUI: C1969038
Disease: RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA (disorder)
RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA (disorder) 		2 0 1 0.12 0 0
CUI: C4016264
Disease: DEJERINE-SOTTAS SYNDROME, AUTOSOMAL DOMINANT
DEJERINE-SOTTAS SYNDROME, AUTOSOMAL DOMINANT 		2 6 1 0.12 1 0.14
CUI: C4721436
Disease: NEUROPATHY, CONGENITAL HYPOMYELINATING, 1, AUTOSOMAL RECESSIVE
NEUROPATHY, CONGENITAL HYPOMYELINATING, 1, AUTOSOMAL RECESSIVE 		2 0 1 0.12 0 0