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: C1846223
Disease: Adrenal hypoplasia
Adrenal hypoplasia 		23 0 1 4.2E-02 0 0
CUI: C1859726
Disease: ARTERIAL TORTUOSITY SYNDROME
ARTERIAL TORTUOSITY SYNDROME 		37 0 1 2.6E-02 0 0
CUI: C3489393
Disease: Hiatal Hernia
Hiatal Hernia 		39 0 1 2.5E-02 0 0
CUI: C0150080
Disease: Social Communication Disorder
Social Communication Disorder 		40 4 1 2.4E-02 1 0.25
CUI: C0266387
Disease: Bicornuate uterus
Bicornuate uterus 		44 0 1 2.2E-02 0 0
CUI: C0034888
Disease: Rectal Prolapse
Rectal Prolapse 		46 0 1 2.1E-02 0 0
CUI: C0206728
Disease: Plexiform Neurofibroma
Plexiform Neurofibroma 		46 0 1 2.1E-02 0 0
CUI: C4551858
Disease: Vesicoureteral Reflux 1
Vesicoureteral Reflux 1 		47 0 1 2.1E-02 0 0
CUI: C0241074
Disease: Hyperextensible skin
Hyperextensible skin 		50 0 1 2.0E-02 0 0
CUI: C2936858
Disease: Congenital adrenal hyperplasia due to 21 hydroxylase deficiency
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency 		50 0 1 2.0E-02 0 0
CUI: C0268287
Disease: Deficiency of steroid 21-monooxygenase
Deficiency of steroid 21-monooxygenase 		54 0 1 1.8E-02 0 0
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency 		55 0 1 1.8E-02 0 0
CUI: C1837352
Disease: Childhood onset
Childhood onset 		56 0 1 1.8E-02 0 0
CUI: C1384494
Disease: Metastatic Carcinoma
Metastatic Carcinoma 		57 0 1 1.7E-02 0 0
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		58 0 1 1.7E-02 0 0
CUI: C0266294
Disease: Unilateral agenesis of kidney
Unilateral agenesis of kidney 		69 0 1 1.4E-02 0 0
CUI: C0947785
Disease: [D]Sleep disturbances (& [hypersomnia] or [insomnia])
[D]Sleep disturbances (& [hypersomnia] or [insomnia]) 		69 0 1 1.4E-02 0 0
CUI: C0014130
Disease: Endocrine System Diseases
Endocrine System Diseases 		74 0 1 1.3E-02 0 0
CUI: C0080174
Disease: Spina Bifida Occulta
Spina Bifida Occulta 		76 0 1 1.3E-02 0 0
CUI: C0013720
Disease: Ehlers-Danlos Syndrome
Ehlers-Danlos Syndrome 		77 0 1 1.3E-02 0 0
CUI: C0423757
Disease: Thin skin
Thin skin 		77 0 1 1.3E-02 0 0
CUI: C0001627
Disease: Congenital adrenal hyperplasia
Congenital adrenal hyperplasia 		87 0 1 1.1E-02 0 0
CUI: C2986658
Disease: Diffuse Intrinsic Pontine Glioma
Diffuse Intrinsic Pontine Glioma 		87 0 1 1.1E-02 0 0
CUI: C0029434
Disease: Osteogenesis Imperfecta
Osteogenesis Imperfecta 		90 0 1 1.1E-02 0 0
CUI: C0010308
Disease: Congenital Hypothyroidism
Congenital Hypothyroidism 		94 48 1 1.1E-02 1 2.1E-02