Source: ALL
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: C0265372
Disease: Fetal hydantoin syndrome
Fetal hydantoin syndrome 		11 0 4 0.12 0 0
CUI: C1096527
Disease: Mosaic trisomy 8 syndrome
Mosaic trisomy 8 syndrome 		4 0 3 0.12 0 0
CUI: C0948391
Disease: Convulsion in childhood
Convulsion in childhood 		5 0 3 0.11 0 0
CUI: C0795940
Disease: Filippi syndrome
Filippi syndrome 		6 0 3 0.11 0 0
CUI: C0392777
Disease: Poikiloderma
Poikiloderma 		20 2 4 9.8E-02 1 4.0E-02
CUI: C0032339
Disease: Rothmund-Thomson syndrome
Rothmund-Thomson syndrome 		35 0 5 9.1E-02 0 0
CUI: C0344191
Disease: Cerebellar decompression injury
Cerebellar decompression injury 		14 0 3 8.3E-02 0 0
CUI: C1313885
Disease: Hereditary edema of legs
Hereditary edema of legs 		2 0 2 8.0E-02 0 0
CUI: C1832334
Disease: CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D 		2 0 2 8.0E-02 0 0
CUI: C2584421
Disease: Postsurgical lymphedema
Postsurgical lymphedema 		2 0 2 8.0E-02 0 0
CUI: C1515091
Disease: Surgically-Created Resection Cavity
Surgically-Created Resection Cavity 		16 0 3 7.9E-02 0 0
CUI: C0235439
Disease: Ankle edema (finding)
Ankle edema (finding) 		4 0 2 7.4E-02 0 0
CUI: C0270970
Disease: Reducing-body myopathy
Reducing-body myopathy 		5 0 2 7.1E-02 0 0
CUI: C0271560
Disease: Lymphocytic hypopituitarism
Lymphocytic hypopituitarism 		5 0 2 7.1E-02 0 0
CUI: C0342410
Disease: Autoimmune Hypophysitis
Autoimmune Hypophysitis 		5 0 2 7.1E-02 0 0
CUI: C0024215
Disease: Lymphangiectasis, Intestinal
Lymphangiectasis, Intestinal 		6 0 2 6.9E-02 0 0
CUI: C0751552
Disease: Malignant neoplasm of thymus
Malignant neoplasm of thymus 		6 0 2 6.9E-02 0 0
CUI: C1835228
Disease: Predominantly lower limb lymphedema
Predominantly lower limb lymphedema 		6 0 2 6.9E-02 0 0
CUI: C4543807
Disease: Clinical malaria
Clinical malaria 		37 0 4 6.9E-02 0 0
CUI: C1112211
Disease: Hepatic Infection
Hepatic Infection 		24 0 3 6.5E-02 0 0
CUI: C1302790
Disease: Congenital malformation syndrome
Congenital malformation syndrome 		57 0 5 6.5E-02 0 0
CUI: C1320453
Disease: Cervical Squamous Cell Carcinoma In Situ
Cervical Squamous Cell Carcinoma In Situ 		10 0 2 6.1E-02 0 0
CUI: C0024214
Disease: Lymphangiectasis
Lymphangiectasis 		11 0 2 5.9E-02 0 0
CUI: C0242594
Disease: Residual Cancer
Residual Cancer 		11 0 2 5.9E-02 0 0
CUI: C0268301
Disease: Reifenstein Syndrome
Reifenstein Syndrome 		11 0 2 5.9E-02 0 0