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: C0337434
Disease: Estradiol measurement
Estradiol measurement
21 0 2 5.7E-02 0 0
CUI: C1443016
Disease: Estradiol level result
Estradiol level result
21 0 2 5.7E-02 0 0
Congenital malformation of the urinary system
3 0 1 5.6E-02 0 0
CUI: C0202100
Disease: Insulin C-peptide measurement
Insulin C-peptide measurement
3 0 1 5.6E-02 0 0
CUI: C0271135
Disease: Ectopic pupil
Ectopic pupil
3 0 1 5.6E-02 0 0
CUI: C1283601
Disease: Deficiency of sulfatase
Deficiency of sulfatase
3 0 1 5.6E-02 0 0
CUI: C1401781
Disease: Short uvula
Short uvula
3 0 1 5.6E-02 0 0
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I
3 0 1 5.6E-02 0 0
CUI: C4522123
Disease: Nerve Growth Factor Measurement
Nerve Growth Factor Measurement
3 0 1 5.6E-02 0 0
CUI: C0028878
Disease: Odontogenesis Imperfecta
Odontogenesis Imperfecta
4 0 1 5.3E-02 0 0
CUI: C0036836
Disease: Serum total protein measurement
Serum total protein measurement
4 0 1 5.3E-02 0 0
Hereditary disturbances in tooth structure, not elsewhere classified in ICD10CM
4 0 1 5.3E-02 0 0
Maturity-Onset Diabetes of the Young, Type 1
4 0 1 5.3E-02 0 0
CUI: C4024867
Disease: Perifollicular hyperkeratosis
Perifollicular hyperkeratosis
4 0 1 5.3E-02 0 0
Decreased level of 1,5 anhydroglucitol in serum
4 0 1 5.3E-02 0 0
Gamma glutamyl transferase measurement
5 0 1 5.0E-02 0 0
CUI: C0428279
Disease: Finding of creatinine level
Finding of creatinine level
5 0 1 5.0E-02 0 0
CUI: C0431693
Disease: Renal cysts and diabetes syndrome
Renal cysts and diabetes syndrome
5 0 1 5.0E-02 0 0
CUI: C1295176
Disease: Leptin measurement
Leptin measurement
5 0 1 5.0E-02 0 0
CUI: C2981132
Disease: Shell teeth
Shell teeth
5 0 1 5.0E-02 0 0
CUI: C0242216
Disease: Biliary calculi
Biliary calculi
48 31 3 4.9E-02 1 2.0E-02
CUI: C0030824
Disease: Allergy to penicillin
Allergy to penicillin
6 0 1 4.8E-02 0 0
CUI: C0036981
Disease: Endotoxic shock
Endotoxic shock
6 0 1 4.8E-02 0 0
CUI: C0085547
Disease: Phenylketonuria, Maternal
Phenylketonuria, Maternal
6 0 1 4.8E-02 0 0
CUI: C0685894
Disease: Congenital absence of thymus
Congenital absence of thymus
6 0 1 4.8E-02 0 0