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: C0850760
Disease: cardiovascular problem
cardiovascular problem 		2 0 1 5.9E-02 0 0
CUI: C0860026
Disease: Leishmania mexicana disease
Leishmania mexicana disease 		2 0 1 5.9E-02 0 0
CUI: C1263722
Disease: Chronic metabolic disorder
Chronic metabolic disorder 		2 0 1 5.9E-02 0 0
CUI: C1836743
Disease: AUDITORY NEUROPATHY, AUTOSOMAL DOMINANT, 1
AUDITORY NEUROPATHY, AUTOSOMAL DOMINANT, 1 		2 0 1 5.9E-02 0 0
CUI: C1846059
Disease: Roifman syndrome
Roifman syndrome 		2 0 1 5.9E-02 0 0
CUI: C1969038
Disease: RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA (disorder)
RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA (disorder) 		2 0 1 5.9E-02 0 0
CUI: C2673809
Disease: Infantile nystagmus
Infantile nystagmus 		2 0 1 5.9E-02 0 0
CUI: C4016701
Disease: INSULIN RESISTANCE, SEVERE, DIGENIC
INSULIN RESISTANCE, SEVERE, DIGENIC 		2 0 1 5.9E-02 0 0
CUI: C0153619
Disease: Malignant neoplasm of ureter
Malignant neoplasm of ureter 		3 0 1 5.6E-02 0 0
CUI: C0271135
Disease: Ectopic pupil
Ectopic pupil 		3 0 1 5.6E-02 0 0
CUI: C0751220
Disease: Inappropriate ACTH Secretion Syndrome
Inappropriate ACTH Secretion Syndrome 		3 0 1 5.6E-02 0 0
CUI: C1401781
Disease: Short uvula
Short uvula 		3 0 1 5.6E-02 0 0
CUI: C1859452
Disease: MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I 		3 0 1 5.6E-02 0 0
CUI: C0009187
Disease: Coccidiosis
Coccidiosis 		4 0 1 5.3E-02 0 0
CUI: C0028878
Disease: Odontogenesis Imperfecta
Odontogenesis Imperfecta 		4 0 1 5.3E-02 0 0
CUI: C0041955
Disease: Ureteral Neoplasms
Ureteral Neoplasms 		4 0 1 5.3E-02 0 0
CUI: C0263222
Disease: Chronic eczema
Chronic eczema 		4 0 1 5.3E-02 0 0
CUI: C0267556
Disease: Osmotic diarrhea
Osmotic diarrhea 		4 0 1 5.3E-02 0 0
CUI: C0494360
Disease: Lipodystrophy, not elsewhere classified
Lipodystrophy, not elsewhere classified 		4 0 1 5.3E-02 0 0
CUI: C0598784
Disease: Dyslipoproteinemias
Dyslipoproteinemias 		24 0 2 5.3E-02 0 0
CUI: C0868847
Disease: Hereditary disturbances in tooth structure, not elsewhere classified in ICD10CM
Hereditary disturbances in tooth structure, not elsewhere classified in ICD10CM 		4 0 1 5.3E-02 0 0
CUI: C1263733
Disease: Uroporphyrinuria
Uroporphyrinuria 		4 0 1 5.3E-02 0 0
CUI: C1299919
Disease: Enteric coccidiosis
Enteric coccidiosis 		4 0 1 5.3E-02 0 0
CUI: C1841679
Disease: Hand foot uterus syndrome
Hand foot uterus syndrome 		4 0 1 5.3E-02 0 0
CUI: C1846013
Disease: Marked muscular hypertrophy
Marked muscular hypertrophy 		4 0 1 5.3E-02 0 0