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: C1866504
Disease: Photosensitive Trichothiodystrophy
Photosensitive Trichothiodystrophy
4 0 1 0.25 0 0
CUI: C4022736
Disease: Impaired social reciprocity
Impaired social reciprocity
6 0 1 0.17 0 0
CUI: C4023792
Disease: Paraplegia/paraparesis
Paraplegia/paraparesis
6 0 1 0.17 0 0
CUI: C4024892
Disease: Congenital exfoliative erythroderma
Congenital exfoliative erythroderma
6 0 1 0.17 0 0
Hypoplasia of mandible relative to maxilla
6 0 1 0.17 0 0
CUI: C4073178
Disease: Tiger tail banding
Tiger tail banding
7 0 1 0.14 0 0
CUI: C0263530
Disease: Longitudinal split nail
Longitudinal split nail
8 0 1 0.12 0 0
CUI: C0423813
Disease: Splits in nails (finding)
Splits in nails (finding)
8 0 1 0.12 0 0
CUI: C1836933
Disease: Low-set nipples
Low-set nipples
9 0 1 0.11 0 0
CUI: C1968565
Disease: Numerous pigmented freckles
Numerous pigmented freckles
9 0 1 0.11 0 0
CUI: C0201512
Disease: Thyroglobulin antibody measurement
Thyroglobulin antibody measurement
10 0 1 1.0E-01 0 0
Recurrent bronchopulmonary infections
10 0 1 1.0E-01 0 0
Xeroderma pigmentosum and Cockayne syndrome complex
10 0 1 1.0E-01 0 0
CUI: C0241267
Disease: Absence of subcutaneous fat
Absence of subcutaneous fat
11 0 1 9.1E-02 0 0
CUI: C1837758
Disease: Bird-like facies
Bird-like facies
12 0 1 8.3E-02 0 0
Defective DNA repair after ultraviolet radiation damage
12 0 1 8.3E-02 0 0
CUI: C4024949
Disease: Generalized hyperreflexia
Generalized hyperreflexia
12 0 1 8.3E-02 0 0
CUI: C0268136
Disease: Xeroderma pigmentosum, group B
Xeroderma pigmentosum, group B
13 0 1 7.7E-02 0 0
Increased mean corpuscular hemoglobin concentration
13 0 1 7.7E-02 0 0
CUI: C0221261
Disease: Koilonychia
Koilonychia
14 0 1 7.1E-02 0 0
CUI: C1859077
Disease: Aplasia/Hypoplasia of the nails
Aplasia/Hypoplasia of the nails
14 0 1 7.1E-02 0 0
CUI: C0574769
Disease: Loss of scalp hair
Loss of scalp hair
16 0 1 6.2E-02 0 0
CUI: C1854699
Disease: Diffuse cerebellar atrophy
Diffuse cerebellar atrophy
17 0 1 5.9E-02 0 0
CUI: C1854885
Disease: Cerebral dysmyelination
Cerebral dysmyelination
17 0 1 5.9E-02 0 0
CUI: C0268141
Disease: Xeroderma pigmentosum, group G
Xeroderma pigmentosum, group G
20 0 1 5.0E-02 0 0