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: C0035091
Disease: Renal Tubular Transport, Inborn Errors
Renal Tubular Transport, Inborn Errors 		1 0 1 2.7E-02 0 0
CUI: C0155002
Disease: Sudden visual loss
Sudden visual loss 		1 0 1 2.7E-02 0 0
CUI: C0232874
Disease: Febrile proteinuria
Febrile proteinuria 		1 0 1 2.7E-02 0 0
CUI: C0342844
Disease: Disorder of glycoprotein metabolism
Disorder of glycoprotein metabolism 		1 0 1 2.7E-02 0 0
CUI: C1622439
Disease: Lentiglobus
Lentiglobus 		1 0 1 2.7E-02 0 0
CUI: C1839874
Disease: Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis
Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis 		1 0 1 2.7E-02 0 0
CUI: C2676786
Disease: Nephrolithiasis-Osteoporosis, Hypophosphatemic, 1
Nephrolithiasis-Osteoporosis, Hypophosphatemic, 1 		1 0 1 2.7E-02 0 0
CUI: C2713392
Disease: Phosphatidylinositol 4,5-Bisphosphate 5-Phosphatase Deficiency
Phosphatidylinositol 4,5-Bisphosphate 5-Phosphatase Deficiency 		1 0 1 2.7E-02 0 0
CUI: C2749861
Disease: MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY)
MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY) 		1 0 1 2.7E-02 0 0
CUI: C2751319
Disease: Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 		1 0 1 2.7E-02 0 0
CUI: C3150172
Disease: MITOCHONDRIAL DNA DEPLETION SYNDROME 8B (MNGIE TYPE)
MITOCHONDRIAL DNA DEPLETION SYNDROME 8B (MNGIE TYPE) 		1 0 1 2.7E-02 0 0
CUI: C3150652
Disease: FANCONI RENOTUBULAR SYNDROME 2
FANCONI RENOTUBULAR SYNDROME 2 		1 0 1 2.7E-02 0 0
CUI: C3278154
Disease: GLUTARIC ACIDEMIA IIA
GLUTARIC ACIDEMIA IIA 		1 0 1 2.7E-02 0 0
CUI: C3278155
Disease: GLUTARIC ACIDEMIA IIB
GLUTARIC ACIDEMIA IIB 		1 0 1 2.7E-02 0 0
CUI: C3278156
Disease: GLUTARIC ACIDEMIA IIC
GLUTARIC ACIDEMIA IIC 		1 0 1 2.7E-02 0 0
CUI: C4016438
Disease: GLUTARIC ACIDEMIA IIC, LATE-ONSET
GLUTARIC ACIDEMIA IIC, LATE-ONSET 		1 0 1 2.7E-02 0 0
CUI: C4016445
Disease: NEPHROLITHIASIS, X-LINKED RECESSIVE
NEPHROLITHIASIS, X-LINKED RECESSIVE 		1 0 1 2.7E-02 0 0
CUI: C4021060
Disease: Hyperplastic labia majora
Hyperplastic labia majora 		1 0 1 2.7E-02 0 0
CUI: C4022041
Disease: Hypoammonemia
Hypoammonemia 		1 0 1 2.7E-02 0 0
CUI: C4022857
Disease: Reduced aldolase level
Reduced aldolase level 		1 0 1 2.7E-02 0 0
CUI: C4022872
Disease: Reduced thyroxin-binding globulin
Reduced thyroxin-binding globulin 		1 0 1 2.7E-02 0 0
CUI: C4024713
Disease: Transient aminoaciduria
Transient aminoaciduria 		1 0 1 2.7E-02 0 0
CUI: C4024767
Disease: Dense posterior cortical cataract
Dense posterior cortical cataract 		1 0 1 2.7E-02 0 0
CUI: C4225421
Disease: LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 3
LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 3 		1 0 1 2.7E-02 0 0
CUI: C4280709
Disease: Impaired neutrophil chemotaxis
Impaired neutrophil chemotaxis 		1 0 1 2.7E-02 0 0