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: C0264878
Disease: Heart valve stenosis
Heart valve stenosis 		1 0 1 8.3E-02 0 0
CUI: C0267827
Disease: Acute toxic hepatitis
Acute toxic hepatitis 		1 0 1 8.3E-02 0 0
CUI: C0278753
Disease: Mesothelioma malignant recurrent
Mesothelioma malignant recurrent 		1 0 1 8.3E-02 0 0
CUI: C0544839
Disease: Macular amyloidosis
Macular amyloidosis 		1 0 1 8.3E-02 0 0
CUI: C0748397
Disease: Reynolds syndrome
Reynolds syndrome 		1 0 1 8.3E-02 0 0
CUI: C0847092
Disease: Blood autoimmune disorders
Blood autoimmune disorders 		1 0 1 8.3E-02 0 0
CUI: C1835253
Disease: Hyperkeratosis over edematous areas
Hyperkeratosis over edematous areas 		1 0 1 8.3E-02 0 0
CUI: C1842797
Disease: Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa of Siemens-like
Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa of Siemens-like 		1 0 1 8.3E-02 0 0
CUI: C1859120
Disease: Anterior rib punctate calcifications
Anterior rib punctate calcifications 		1 0 1 8.3E-02 0 0
CUI: C1859121
Disease: Sternal punctate calcifications
Sternal punctate calcifications 		1 0 1 8.3E-02 0 0
CUI: C1866048
Disease: Severe hydrops fetalis
Severe hydrops fetalis 		1 0 1 8.3E-02 0 0
CUI: C2750784
Disease: SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE (disorder)
SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE (disorder) 		1 0 1 8.3E-02 0 0
CUI: C2930842
Disease: Familial pityriasis rubra pilaris
Familial pityriasis rubra pilaris 		1 0 1 8.3E-02 0 0
CUI: C3179244
Disease: Pseudo Pelger-Huet Anomaly
Pseudo Pelger-Huet Anomaly 		1 0 1 8.3E-02 0 0
CUI: C4017074
Disease: PSORIASIS 2, PUSTULAR
PSORIASIS 2, PUSTULAR 		1 0 1 8.3E-02 0 0
CUI: C4021245
Disease: Patchy variation in bone mineral density
Patchy variation in bone mineral density 		1 0 1 8.3E-02 0 0
CUI: C4025570
Disease: Hypoplasia of lymphatic vessels
Hypoplasia of lymphatic vessels 		1 0 1 8.3E-02 0 0
CUI: C4025815
Disease: Short diaphyses
Short diaphyses 		1 0 1 8.3E-02 0 0
CUI: C4225407
Disease: PEELING SKIN SYNDROME 4
PEELING SKIN SYNDROME 4 		1 0 1 8.3E-02 0 0
CUI: C4273658
Disease: Graham Little Piccardi Lassueur syndrome
Graham Little Piccardi Lassueur syndrome 		1 0 1 8.3E-02 0 0
CUI: C4725868
Disease: Resectable Dedifferentiated Liposarcoma
Resectable Dedifferentiated Liposarcoma 		1 0 1 8.3E-02 0 0
CUI: C4747646
Disease: LYMPHATIC MALFORMATION 3
LYMPHATIC MALFORMATION 3 		1 0 1 8.3E-02 0 0
CUI: C4747769
Disease: LYMPHATIC MALFORMATION 4
LYMPHATIC MALFORMATION 4 		1 0 1 8.3E-02 0 0
CUI: C4747922
Disease: PELGER-HUET ANOMALY WITH MILD SKELETAL ANOMALIES
PELGER-HUET ANOMALY WITH MILD SKELETAL ANOMALIES 		1 0 1 8.3E-02 0 0
CUI: C0001361
Disease: Acute tonsillitis
Acute tonsillitis 		2 0 1 7.7E-02 0 0