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: C0235439
Disease: Ankle edema (finding)
Ankle edema (finding)
4 0 3 0.43 0 0
CUI: C0238261
Disease: Lymphedema praecox
Lymphedema praecox
9 0 4 0.36 0 0
CUI: C1313885
Disease: Hereditary edema of legs
Hereditary edema of legs
2 0 2 0.33 0 0
CUI: C2584421
Disease: Postsurgical lymphedema
Postsurgical lymphedema
2 0 2 0.33 0 0
CUI: C3276623
Disease: Toenail dysplasia
Toenail dysplasia
13 0 4 0.27 0 0
CUI: C0024214
Disease: Lymphangiectasis
Lymphangiectasis
11 0 3 0.21 0 0
CUI: C0023653
Disease: Lichenification
Lichenification
12 0 3 0.20 0 0
Lichenification and lichen simplex chronicus
12 0 3 0.20 0 0
CUI: C0024215
Disease: Lymphangiectasis, Intestinal
Lymphangiectasis, Intestinal
6 0 2 0.20 0 0
CUI: C1720771
Disease: Testicular Hydrocele
Testicular Hydrocele
21 0 4 0.17 0 0
CUI: C1704424
Disease: Hereditary lymphedema type II
Hereditary lymphedema type II
1 0 1 0.17 0 0
CUI: C1708341
Disease: Heavier Menses
Heavier Menses
1 0 1 0.17 0 0
CUI: C1835253
Disease: Hyperkeratosis over edematous areas
Hyperkeratosis over edematous areas
1 0 1 0.17 0 0
HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA SYNDROME
1 0 1 0.17 0 0
Cerebellar Ataxia, Deafness, and Narcolepsy
1 0 1 0.17 0 0
Lymphedema-Distichiasis Syndrome with Renal Disease and Diabetes Mellitus
1 0 1 0.17 0 0
SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE (disorder)
1 0 1 0.17 0 0
Hereditary Sensory and Autonomic Neuropathy Type Ie
1 0 1 0.17 0 0
CUI: C4020947
Disease: Plantar telangiectasia
Plantar telangiectasia
1 0 1 0.17 0 0
CUI: C4021393
Disease: Spinalarachnoid cyst
Spinalarachnoid cyst
1 0 1 0.17 0 0
CUI: C4021653
Disease: Generalized hypotrichosis
Generalized hypotrichosis
1 0 1 0.17 0 0
CUI: C4024827
Disease: Telangiectasia of extensor surfaces
Telangiectasia of extensor surfaces
1 0 1 0.17 0 0
CUI: C4025570
Disease: Hypoplasia of lymphatic vessels
Hypoplasia of lymphatic vessels
1 0 1 0.17 0 0
Hypotrichosis, lymphedema, telangiectasia, renal defect syndrome
1 0 1 0.17 0 0
CUI: C4747646
Disease: LYMPHATIC MALFORMATION 3
LYMPHATIC MALFORMATION 3
1 0 1 0.17 0 0