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: C1837108
Disease: Decreased muscle mass
Decreased muscle mass
65 0 21 0.14 0 0
CUI: C1866195
Disease: Downturned corners of mouth
Downturned corners of mouth
122 0 26 0.13 0 0
CUI: C0020505
Disease: Hyperphagia
Hyperphagia
60 0 18 0.12 0 0
CUI: C1837522
Disease: Impaired pain sensation
Impaired pain sensation
41 0 16 0.12 0 0
CUI: C1857632
Disease: Narrow palm
Narrow palm
17 0 13 0.11 0 0
CUI: C4551564
Disease: Narrow nasal bridge
Narrow nasal bridge
47 0 16 0.11 0 0
CUI: C0265222
Disease: Royer Syndrome
Royer Syndrome
12 0 12 0.11 0 0
CUI: C1386091
Disease: Acromicria
Acromicria
13 0 12 0.11 0 0
CUI: C0028949
Disease: Oligomenorrhea
Oligomenorrhea
37 0 14 0.10 0 0
CUI: C0271561
Disease: Somatotropin deficiency
Somatotropin deficiency
154 0 25 0.10 0 0
CUI: C0544886
Disease: Somatic mutation
Somatic mutation
151 0 24 0.10 0 0
CUI: C0265287
Disease: Acromicric Dysplasia
Acromicric Dysplasia
21 0 12 1.0E-01 0 0
CUI: C0311277
Disease: Obesity, Abdominal
Obesity, Abdominal
21 0 12 1.0E-01 0 0
CUI: C1843108
Disease: Short palm
Short palm
110 0 20 1.0E-01 0 0
CUI: C0556280
Disease: Gross motor impairment
Gross motor impairment
22 0 12 9.9E-02 0 0
CUI: C3714796
Disease: Isolated somatotropin deficiency
Isolated somatotropin deficiency
168 0 25 9.8E-02 0 0
CUI: C1849923
Disease: Generalized hypopigmentation
Generalized hypopigmentation
23 0 12 9.8E-02 0 0
CUI: C4025790
Disease: Specific learning disability
Specific learning disability
165 0 24 9.5E-02 0 0
CUI: C0221263
Disease: Cafe-au-Lait Spots
Cafe-au-Lait Spots
74 0 16 9.5E-02 0 0
CUI: C3203358
Disease: Hypoventilation
Hypoventilation
28 0 12 9.4E-02 0 0
CUI: C1844527
Disease: Clitoral hypoplasia
Clitoral hypoplasia
30 0 12 9.3E-02 0 0
CUI: C1849295
Disease: Hypoplastic labia minora
Hypoplastic labia minora
30 0 12 9.3E-02 0 0
CUI: C0431659
Disease: Hypoplasia of scrotum
Hypoplasia of scrotum
57 0 14 9.1E-02 0 0
CUI: C0221358
Disease: Long narrow head
Long narrow head
154 0 22 9.1E-02 0 0
CUI: C0038271
Disease: Stereotyped Behavior
Stereotyped Behavior
135 0 20 8.8E-02 0 0