Source: BEFREE ×
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: C0013336
Disease: Dwarfism
Dwarfism 		377 64 29 7.4E-02 7 9.7E-02
CUI: C0271801
Disease: Central hypothyroidism
Central hypothyroidism 		27 0 5 7.4E-02 0 0
CUI: C1837475
Disease: Insulin-Like Growth Factor I Deficiency
Insulin-Like Growth Factor I Deficiency 		27 0 5 7.4E-02 0 0
CUI: C2931196
Disease: Craniofacial dysostosis type 1
Craniofacial dysostosis type 1 		13 29 4 7.3E-02 1 2.3E-02
CUI: C0026707
Disease: Mucopolysaccharidosis IV
Mucopolysaccharidosis IV 		28 0 5 7.2E-02 0 0
CUI: C1857941
Disease: Brooke-Spiegler syndrome
Brooke-Spiegler syndrome 		43 0 6 7.2E-02 0 0
CUI: C0028326
Disease: Noonan Syndrome
Noonan Syndrome 		77 0 8 7.0E-02 0 0
CUI: C2745963
Disease: Kashin-Beck Disease
Kashin-Beck Disease 		77 0 8 7.0E-02 0 0
CUI: C0333291
Disease: Bleeding ulcer
Bleeding ulcer 		16 0 4 6.9E-02 0 0
CUI: C0023798
Disease: Lipoma
Lipoma 		63 0 7 6.9E-02 0 0
CUI: C0013338
Disease: Pituitary dwarfism
Pituitary dwarfism 		33 0 5 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: C0020455
Disease: Hypergammaglobulinemia
Hypergammaglobulinemia 		35 0 5 6.6E-02 0 0
CUI: C0333317
Disease: Fibrous body
Fibrous body 		3 0 3 6.5E-02 0 0
CUI: C3489413
Disease: Lipomatosis, Multiple
Lipomatosis, Multiple 		52 0 6 6.5E-02 0 0
CUI: C0266541
Disease: Microphakia
Microphakia 		4 0 3 6.4E-02 0 0
CUI: C1864356
Disease: ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE
ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE 		4 0 3 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: C0175695
Disease: Sotos' syndrome
Sotos' syndrome 		21 0 4 6.3E-02 0 0
CUI: C0265269
Disease: Lacrimoauriculodentodigital syndrome
Lacrimoauriculodentodigital syndrome 		5 0 3 6.2E-02 0 0
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: C3540852
Disease: Rickets, X-Linked Hypophosphatemic
Rickets, X-Linked Hypophosphatemic 		22 0 4 6.2E-02 0 0
CUI: C4316913
Disease: Autoimmune Polyglandular Syndrome
Autoimmune Polyglandular Syndrome 		5 0 3 6.2E-02 0 0
CUI: C0027859
Disease: Acoustic Neuroma
Acoustic Neuroma 		126 0 10 6.2E-02 0 0
CUI: C1282952
Disease: Enthesitis
Enthesitis 		23 0 4 6.2E-02 0 0