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: C0342162
Disease: Compensated hypothyroidism
Compensated hypothyroidism
7 0 2 7.1E-02 0 0
CUI: C2676974
Disease: Hypoplasia of the cochlea
Hypoplasia of the cochlea
7 0 2 7.1E-02 0 0
CUI: C0037889
Disease: Hereditary spherocytosis
Hereditary spherocytosis
53 13 5 7.0E-02 1 3.3E-02
CUI: C0025237
Disease: Melnick-Needles Syndrome
Melnick-Needles Syndrome
23 0 3 7.0E-02 0 0
Ovalocytosis, Malaysian-Melanesian-Filipino Type
9 5 2 6.7E-02 4 0.21
CUI: C4021553
Disease: Periodic hypokalemic paresis
Periodic hypokalemic paresis
9 0 2 6.7E-02 0 0
DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT
10 0 2 6.5E-02 0 0
CUI: C0220983
Disease: Metabolic alkalosis
Metabolic alkalosis
27 0 3 6.4E-02 0 0
CUI: C0342191
Disease: Familial dyshormonogenetic goiter
Familial dyshormonogenetic goiter
11 0 2 6.2E-02 0 0
CUI: C0027709
Disease: Nephrocalcinosis
Nephrocalcinosis
118 0 8 6.0E-02 0 0
CUI: C0001127
Disease: Acidosis, Respiratory
Acidosis, Respiratory
13 0 2 5.9E-02 0 0
CUI: C0041466
Disease: Typhoid Fever
Typhoid Fever
31 0 3 5.9E-02 0 0
CUI: C0403367
Disease: proliferative nephritis unspecified
proliferative nephritis unspecified
14 0 2 5.7E-02 0 0
CUI: C0346255
Disease: Oncocytoma, renal
Oncocytoma, renal
34 0 3 5.6E-02 0 0
Extramedullary Hematopoiesis Function
16 0 2 5.4E-02 0 0
CUI: C1843865
Disease: Vestibular dysfunction
Vestibular dysfunction
16 0 2 5.4E-02 0 0
CUI: C0022610
Disease: Kernicterus
Kernicterus
17 0 2 5.3E-02 0 0
CUI: C0339467
Disease: Proliferative retinopathy
Proliferative retinopathy
57 0 4 5.3E-02 0 0
DEAFNESS, AUTOSOMAL RECESSIVE (disorder)
38 0 3 5.2E-02 0 0
CUI: C0019045
Disease: Hemoglobinopathies
Hemoglobinopathies
80 0 5 5.1E-02 0 0
Malignant hyperpyrexia due to anesthesia
60 0 4 5.1E-02 0 0
CUI: C0410538
Disease: Pseudoachondroplasia
Pseudoachondroplasia
19 0 2 5.0E-02 0 0
CUI: C0022716
Disease: Menkes Kinky Hair Syndrome
Menkes Kinky Hair Syndrome
20 0 2 4.9E-02 0 0
CUI: C0272051
Disease: Xerocytosis
Xerocytosis
20 0 2 4.9E-02 0 0
Diffuse mesangial sclerosis (disorder)
22 0 2 4.7E-02 0 0