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: C1856231
Disease: Thin calvarium
Thin calvarium 		1 0 1 4.5E-02 0 0
CUI: C1864861
Disease: Tumoral Calcinosis, Normophosphatemic, Familial
Tumoral Calcinosis, Normophosphatemic, Familial 		1 0 1 4.5E-02 0 0
CUI: C1866182
Disease: Penttinen-Aula syndrome
Penttinen-Aula syndrome 		1 0 1 4.5E-02 0 0
CUI: C1955858
Disease: Deaf-Blind Syndromes
Deaf-Blind Syndromes 		1 0 1 4.5E-02 0 0
CUI: C1960052
Disease: Chronic hypercapnic respiratory failure
Chronic hypercapnic respiratory failure 		1 0 1 4.5E-02 0 0
CUI: C2242813
Disease: Ranula (disorder)
Ranula (disorder) 		1 0 1 4.5E-02 0 0
CUI: C2584751
Disease: Severe hereditary factor VIII deficiency disease without inhibitor
Severe hereditary factor VIII deficiency disease without inhibitor 		1 0 1 4.5E-02 0 0
CUI: C2677524
Disease: Hypophosphatemic Rickets And Hyperparathyroidism
Hypophosphatemic Rickets And Hyperparathyroidism 		1 0 1 4.5E-02 0 0
CUI: C2931105
Disease: Hypercalciuria, childhood idiopathic
Hypercalciuria, childhood idiopathic 		1 0 1 4.5E-02 0 0
CUI: C3149907
Disease: AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 13
AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 13 		1 0 1 4.5E-02 0 0
CUI: C3203502
Disease: Hyperactive delirium
Hyperactive delirium 		1 0 1 4.5E-02 0 0
CUI: C3472621
Disease: Myeloid neoplasm with beta-type platelet-derived growth factor receptor gene rearrangement
Myeloid neoplasm with beta-type platelet-derived growth factor receptor gene rearrangement 		1 0 1 4.5E-02 0 0
CUI: C3532225
Disease: Valvular cardiomyopathy
Valvular cardiomyopathy 		1 0 1 4.5E-02 0 0
CUI: C3554321
Disease: BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 4
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 4 		1 3 1 4.5E-02 1 0.33
CUI: C3711560
Disease: Pdgfrb-Associated Chronic Eosinophilic Leukemia
Pdgfrb-Associated Chronic Eosinophilic Leukemia 		1 0 1 4.5E-02 0 0
CUI: C4015525
Disease: LISSENCEPHALY 6 WITH MICROCEPHALY
LISSENCEPHALY 6 WITH MICROCEPHALY 		1 0 1 4.5E-02 0 0
CUI: C4015884
Disease: DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL RECESSIVE
DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL RECESSIVE 		1 0 1 4.5E-02 0 0
CUI: C4015885
Disease: DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL DOMINANT
DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL DOMINANT 		1 0 1 4.5E-02 0 0
CUI: C4023340
Disease: Childhood onset sensorineural hearing impairment
Childhood onset sensorineural hearing impairment 		1 0 1 4.5E-02 0 0
CUI: C4087267
Disease: Bendopnoea
Bendopnoea 		1 0 1 4.5E-02 0 0
CUI: C4303980
Disease: Acute on chronic hypercapnic respiratory failure
Acute on chronic hypercapnic respiratory failure 		1 0 1 4.5E-02 0 0
CUI: C4518466
Disease: Stroke co-occurrent with migraine
Stroke co-occurrent with migraine 		1 0 1 4.5E-02 0 0
CUI: C4551572
Disease: MYOFIBROMATOSIS, INFANTILE, 1
MYOFIBROMATOSIS, INFANTILE, 1 		1 0 1 4.5E-02 0 0
CUI: C4693864
Disease: TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 3
TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 3 		1 0 1 4.5E-02 0 0
CUI: C4748869
Disease: MIRROR MOVEMENTS 4
MIRROR MOVEMENTS 4 		1 0 1 4.5E-02 0 0