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: C0235584
Disease: Granulocytopenia severe
Granulocytopenia severe 		1 0 1 5.6E-02 0 0
CUI: C0272404
Disease: Hyposplenism
Hyposplenism 		1 0 1 5.6E-02 0 0
CUI: C0276742
Disease: Kerion celsi
Kerion celsi 		1 0 1 5.6E-02 0 0
CUI: C0282002
Disease: Superficial Infection
Superficial Infection 		1 0 1 5.6E-02 0 0
CUI: C0333419
Disease: Sarcoid type granuloma
Sarcoid type granuloma 		1 0 1 5.6E-02 0 0
CUI: C0341248
Disease: Chronic duodenitis
Chronic duodenitis 		1 0 1 5.6E-02 0 0
CUI: C0595928
Disease: Serum calcium increased
Serum calcium increased 		1 0 1 5.6E-02 0 0
CUI: C1611171
Disease: Thalamic infarction
Thalamic infarction 		1 0 1 5.6E-02 0 0
CUI: C1820738
Disease: Feeding intolerance
Feeding intolerance 		1 0 1 5.6E-02 0 0
CUI: C1832612
Disease: Hypocalcemia, Autosomal Dominant, with Bartter Syndrome
Hypocalcemia, Autosomal Dominant, with Bartter Syndrome 		1 0 1 5.6E-02 0 0
CUI: C1832827
Disease: DEAFNESS, CHILDHOOD-ONSET NEUROSENSORY, AUTOSOMAL RECESSIVE 8
DEAFNESS, CHILDHOOD-ONSET NEUROSENSORY, AUTOSOMAL RECESSIVE 8 		1 0 1 5.6E-02 0 0
CUI: C1844663
Disease: ISLETS OF LANGERHANS, ABSENCE OF
ISLETS OF LANGERHANS, ABSENCE OF 		1 0 1 5.6E-02 0 0
CUI: C1853104
Disease: ALOPECIA AREATA 2
ALOPECIA AREATA 2 		1 0 1 5.6E-02 0 0
CUI: C1855868
Disease: Polyglandular Deficiency Syndrome, Persian-Jewish Type
Polyglandular Deficiency Syndrome, Persian-Jewish Type 		1 0 1 5.6E-02 0 0
CUI: C1855869
Disease: Autoimmune Polyendocrinopathy Syndrome, Type I, Autosomal Dominant
Autoimmune Polyendocrinopathy Syndrome, Type I, Autosomal Dominant 		1 0 1 5.6E-02 0 0
CUI: C1960561
Disease: Hemidystonia
Hemidystonia 		1 0 1 5.6E-02 0 0
CUI: C1970472
Disease: PULMONARY ALVEOLAR PROTEINOSIS, ACQUIRED
PULMONARY ALVEOLAR PROTEINOSIS, ACQUIRED 		1 0 1 5.6E-02 0 0
CUI: C2749602
Disease: AUTOIMMUNE POLYENDOCRINOPATHY SYNDROME, TYPE I, WITH REVERSIBLE METAPHYSEAL DYSPLASIA
AUTOIMMUNE POLYENDOCRINOPATHY SYNDROME, TYPE I, WITH REVERSIBLE METAPHYSEAL DYSPLASIA 		1 0 1 5.6E-02 0 0
CUI: C2752062
Disease: EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 8
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 8 		1 0 1 5.6E-02 0 0
CUI: C3151405
Disease: CANDIDIASIS, FAMILIAL, 6
CANDIDIASIS, FAMILIAL, 6 		1 0 1 5.6E-02 0 0
CUI: C3863587
Disease: enterovirus d68 infection
enterovirus d68 infection 		1 0 1 5.6E-02 0 0
CUI: C3888929
Disease: Cryptococcus gattii infection
Cryptococcus gattii infection 		1 0 1 5.6E-02 0 0
CUI: C4293676
Disease: Anti-liver cytosolic antigen type 1 antibody positivity
Anti-liver cytosolic antigen type 1 antibody positivity 		1 0 1 5.6E-02 0 0
CUI: C4476964
Disease: Decreased prealbumin level
Decreased prealbumin level 		1 0 1 5.6E-02 0 0
CUI: C4531149
Disease: Reduced proportion of CD4-negative, CD8-negative, alpha-beta regulatory T cells
Reduced proportion of CD4-negative, CD8-negative, alpha-beta regulatory T cells 		1 0 1 5.6E-02 0 0