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: C0860439
Disease: Mottled pigmentation
Mottled pigmentation
5 0 2 8.0E-02 0 0
Insulin-resistant diabetes mellitus at puberty
5 0 2 8.0E-02 0 0
CUI: C4023965
Disease: Structural foot deformity
Structural foot deformity
5 0 2 8.0E-02 0 0
CUI: C4024993
Disease: Aplasia/Hypoplasia of the clavicles
Aplasia/Hypoplasia of the clavicles
5 0 2 8.0E-02 0 0
CUI: C1846438
Disease: Hypoplastic facial bones
Hypoplastic facial bones
6 0 2 7.7E-02 0 0
CUI: C1856542
Disease: Prominent scalp veins
Prominent scalp veins
6 0 2 7.7E-02 0 0
CUI: C1856714
Disease: Palmoplantar cutis laxa
Palmoplantar cutis laxa
6 0 2 7.7E-02 0 0
CUI: C3276815
Disease: Stiff skin
Stiff skin
6 0 2 7.7E-02 0 0
CUI: C4020957
Disease: Abnormal trabecular bone morphology
Abnormal trabecular bone morphology
6 0 2 7.7E-02 0 0
CUI: C3810018
Disease: Bilateral coxa valga
Bilateral coxa valga
7 0 2 7.4E-02 0 0
CUI: C3279575
Disease: Reticulated skin pigmentation
Reticulated skin pigmentation
8 0 2 7.1E-02 0 0
Aplasia/Hypoplasia involving the nose
8 0 2 7.1E-02 0 0
Familial Partial Lipodystrophy, Type 1
9 0 2 6.9E-02 0 0
CUI: C1867114
Disease: Craniofacial disproportion
Craniofacial disproportion
9 0 2 6.9E-02 0 0
CUI: C0423823
Disease: Thin nails
Thin nails
10 0 2 6.7E-02 0 0
Familial Partial Lipodystrophy, Type 3
10 0 2 6.7E-02 0 0
CUI: C1833762
Disease: Decreased calvarial ossification
Decreased calvarial ossification
10 0 2 6.7E-02 0 0
CUI: C1836646
Disease: Dermal translucency
Dermal translucency
10 0 2 6.7E-02 0 0
CUI: C0266200
Disease: Microcolon
Microcolon
11 0 2 6.5E-02 0 0
CUI: C1837761
Disease: Narrow nasal ridge
Narrow nasal ridge
11 0 2 6.5E-02 0 0
Loss of subcutaneous adipose tissue in limbs
11 0 2 6.5E-02 0 0
CUI: C1851792
Disease: Aplasia/Hypoplasia of the earlobes
Aplasia/Hypoplasia of the earlobes
11 0 2 6.5E-02 0 0
HIV-Associated Lipodystrophy Syndrome
12 0 2 6.2E-02 0 0
CUI: C1837758
Disease: Bird-like facies
Bird-like facies
12 0 2 6.2E-02 0 0
CUI: C1318518
Disease: Infantile malignant osteopetrosis
Infantile malignant osteopetrosis
13 0 2 6.1E-02 0 0