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: C0271789
Disease: Hypothyroidism, Congenital, Nongoitrous, 4
Hypothyroidism, Congenital, Nongoitrous, 4 		2 0 1 0.50 0 0
CUI: C0022346
Disease: Icterus
Icterus 		241 0 1 4.1E-03 0 0
CUI: C1846149
Disease: Intellectual disability, progressive
Intellectual disability, progressive 		45 0 1 2.2E-02 0 0
CUI: C0456132
Disease: Large fontanelle
Large fontanelle 		77 0 1 1.3E-02 0 0
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		5725 0 1 1.7E-04 0 0
CUI: C0024421
Disease: Macroglossia
Macroglossia 		115 0 1 8.7E-03 0 0
CUI: C0338831
Disease: Manic
Manic 		166 0 1 6.0E-03 0 0
CUI: C0024713
Disease: Manic Disorder
Manic Disorder 		76 0 1 1.3E-02 0 0
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		967 0 1 1.0E-03 0 0
CUI: C0027651
Disease: Neoplasms
Neoplasms 		10161 0 1 9.8E-05 0 0
CUI: C0085215
Disease: Ovarian Failure, Premature
Ovarian Failure, Premature 		333 0 1 3.0E-03 0 0
CUI: C0032002
Disease: Pituitary Diseases
Pituitary Diseases 		153 0 1 6.5E-03 0 0
CUI: C0025322
Disease: Premature Menopause
Premature Menopause 		299 0 1 3.3E-03 0 0
CUI: C4316995
Disease: Primary Hypothyroidism
Primary Hypothyroidism 		19 0 1 5.3E-02 0 0
CUI: C0860634
Disease: Psychogenic coma
Psychogenic coma 		5 0 1 0.20 0 0
CUI: C3665349
Disease: Secondary hypothyroidism
Secondary hypothyroidism 		47 0 1 2.1E-02 0 0
CUI: C0036857
Disease: Severe intellectual disability
Severe intellectual disability 		429 0 1 2.3E-03 0 0
CUI: C1857641
Disease: Severe postnatal growth retardation
Severe postnatal growth retardation 		30 0 1 3.3E-02 0 0
CUI: C0851578
Disease: Sleep Disorders
Sleep Disorders 		360 0 1 2.8E-03 0 0
CUI: C0037317
Disease: Sleep disturbances
Sleep disturbances 		311 0 1 3.2E-03 0 0
CUI: C1563716
Disease: Thyroid Dysgenesis
Thyroid Dysgenesis 		24 0 1 4.2E-02 0 0
CUI: C4082174
Disease: Thyrotropin deficiency, isolated
Thyrotropin deficiency, isolated 		1 0 1 1.00 0 0
CUI: C0041408
Disease: Turner Syndrome
Turner Syndrome 		162 0 1 6.2E-03 0 0
CUI: C1866134
Disease: Wide anterior fontanel
Wide anterior fontanel 		71 0 1 1.4E-02 0 0