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: C0020514
Disease: Hyperprolactinemia
Hyperprolactinemia 		48 0 6 6.8E-02 0 0
CUI: C1333295
Disease: Diffuse Large B-Cell Lymphoma Germinal Center B-Cell Type
Diffuse Large B-Cell Lymphoma Germinal Center B-Cell Type 		18 0 4 6.7E-02 0 0
CUI: C0271801
Disease: Central hypothyroidism
Central hypothyroidism 		35 0 5 6.6E-02 0 0
CUI: C1561989
Disease: Limbal stem cell deficiency
Limbal stem cell deficiency 		19 0 4 6.6E-02 0 0
CUI: C0333317
Disease: Fibrous body
Fibrous body 		3 0 3 6.5E-02 0 0
CUI: C0028326
Disease: Noonan Syndrome
Noonan Syndrome 		85 0 8 6.5E-02 0 0
CUI: C0020455
Disease: Hypergammaglobulinemia
Hypergammaglobulinemia 		36 0 5 6.5E-02 0 0
CUI: C0878659
Disease: Disproportionate short stature
Disproportionate short stature 		86 0 8 6.5E-02 0 0
CUI: C0271561
Disease: Somatotropin deficiency
Somatotropin deficiency 		154 0 12 6.4E-02 0 0
CUI: C1858569
Disease: Absence of Stensen duct
Absence of Stensen duct 		4 0 3 6.4E-02 0 0
CUI: C3489413
Disease: Lipomatosis, Multiple
Lipomatosis, Multiple 		54 0 6 6.4E-02 0 0
CUI: C4543877
Disease: Osteopenia due to disuse
Osteopenia due to disuse 		4 0 3 6.4E-02 0 0
CUI: C0029422
Disease: Osteochondrodysplasias
Osteochondrodysplasias 		207 26 15 6.3E-02 3 6.8E-02
CUI: C0014084
Disease: Enchondromatosis
Enchondromatosis 		22 0 4 6.2E-02 0 0
CUI: C0206720
Disease: Squamous Cell Neoplasms
Squamous Cell Neoplasms 		22 0 4 6.2E-02 0 0
CUI: C0265269
Disease: Lacrimoauriculodentodigital syndrome
Lacrimoauriculodentodigital syndrome 		5 33 3 6.2E-02 7 0.15
CUI: C0266184
Disease: Congenital duodenal obstruction due to malrotation of intestine
Congenital duodenal obstruction due to malrotation of intestine 		5 0 3 6.2E-02 0 0
CUI: C1864356
Disease: ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE
ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE 		5 0 3 6.2E-02 0 0
CUI: C4023357
Disease: Maternal teratogenic exposure
Maternal teratogenic exposure 		5 0 3 6.2E-02 0 0
CUI: C4316811
Disease: Abnormality of the nasal septum
Abnormality of the nasal septum 		5 0 3 6.2E-02 0 0
CUI: C4316913
Disease: Autoimmune Polyglandular Syndrome
Autoimmune Polyglandular Syndrome 		5 0 3 6.2E-02 0 0
CUI: C1184923
Disease: Lumbar hyperlordosis
Lumbar hyperlordosis 		92 0 8 6.2E-02 0 0
CUI: C3540852
Disease: Rickets, X-Linked Hypophosphatemic
Rickets, X-Linked Hypophosphatemic 		23 0 4 6.2E-02 0 0
CUI: C0026916
Disease: Mycobacterium avium-intracellulare Infection
Mycobacterium avium-intracellulare Infection 		58 0 6 6.1E-02 0 0
CUI: C0266541
Disease: Microphakia
Microphakia 		6 0 3 6.1E-02 0 0