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: C0037188
Disease: Sinoatrial Block
Sinoatrial Block 		1 0 1 0.25 0 0
CUI: C0270709
Disease: Rud Syndrome
Rud Syndrome 		1 0 1 0.25 0 0
CUI: C0339295
Disease: Exposure keratoconjunctivitis
Exposure keratoconjunctivitis 		1 0 1 0.25 0 0
CUI: C0796031
Disease: Malouf syndrome
Malouf syndrome 		1 0 1 0.25 0 0
CUI: C0796083
Disease: Najjar syndrome
Najjar syndrome 		1 0 1 0.25 0 0
CUI: C1304147
Disease: Retention hyperkeratosis
Retention hyperkeratosis 		1 0 1 0.25 0 0
CUI: C1835380
Disease: Labial pseudohypertrophy
Labial pseudohypertrophy 		1 0 1 0.25 0 0
CUI: C1835389
Disease: Increased intramuscular fat
Increased intramuscular fat 		1 0 1 0.25 0 0
CUI: C1857829
Disease: Heart-hand syndrome, Slovenian type
Heart-hand syndrome, Slovenian type 		1 0 1 0.25 0 0
CUI: C2675074
Disease: Enlarged peripheral nerve
Enlarged peripheral nerve 		1 0 1 0.25 0 0
CUI: C2750035
Disease: Emery-Dreifuss Muscular Dystrophy 3
Emery-Dreifuss Muscular Dystrophy 3 		1 0 1 0.25 0 0
CUI: C2750285
Disease: Progeria Syndrome, Childhood-Onset
Progeria Syndrome, Childhood-Onset 		1 0 1 0.25 0 0
CUI: C2750785
Disease: MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder)
MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder) 		1 0 1 0.25 0 0
CUI: C4016241
Disease: HUTCHINSON-GILFORD PROGERIA SYNDROME, ATYPICAL
HUTCHINSON-GILFORD PROGERIA SYNDROME, ATYPICAL 		1 0 1 0.25 0 0
CUI: C4021684
Disease: Sclerosis of hand bone
Sclerosis of hand bone 		1 0 1 0.25 0 0
CUI: C4022125
Disease: Aplasia of the phalanges of the 3rd toe
Aplasia of the phalanges of the 3rd toe 		1 0 1 0.25 0 0
CUI: C4023222
Disease: Abnormal electrophysiology of sinoatrial node origin
Abnormal electrophysiology of sinoatrial node origin 		1 0 1 0.25 0 0
CUI: C4025339
Disease: Abnormality of circulating leptin level
Abnormality of circulating leptin level 		1 0 1 0.25 0 0
CUI: C4025868
Disease: Increased facial adipose tissue
Increased facial adipose tissue 		1 0 1 0.25 0 0
CUI: C4229131
Disease: Distal acroosteolysis
Distal acroosteolysis 		1 0 1 0.25 0 0
CUI: C4274085
Disease: Syndromic recessive X-linked ichthyosis
Syndromic recessive X-linked ichthyosis 		1 0 1 0.25 0 0
CUI: C4531142
Disease: Abnormal lymphocyte physiology
Abnormal lymphocyte physiology 		1 0 1 0.25 0 0
CUI: C4750858
Disease: LMNA-related cardiocutaneous progeria syndrome
LMNA-related cardiocutaneous progeria syndrome 		1 0 1 0.25 0 0
CUI: C0155196
Disease: Cicatricial ectropion
Cicatricial ectropion 		2 0 1 0.20 0 0
CUI: C0339282
Disease: Pre-descemet's corneal dystrophy
Pre-descemet's corneal dystrophy 		2 0 1 0.20 0 0