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: C0020538
Disease: Hypertensive disease
Hypertensive disease 		2322 1085 6 2.6E-03 1 9.1E-04
CUI: C0014544
Disease: Epilepsy
Epilepsy 		1215 339 4 3.3E-03 1 2.8E-03
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		613 283 7 1.1E-02 3 1.0E-02
CUI: C2315100
Disease: Pediatric failure to thrive
Pediatric failure to thrive 		166 122 2 1.2E-02 1 7.1E-03
CUI: C0038379
Disease: Strabismus
Strabismus 		716 89 3 4.2E-03 1 9.3E-03
CUI: C0424605
Disease: Developmental delay (disorder)
Developmental delay (disorder) 		584 68 3 5.1E-03 1 1.2E-02
CUI: C0010308
Disease: Congenital Hypothyroidism
Congenital Hypothyroidism 		94 48 5 5.1E-02 3 4.7E-02
CUI: C4722330
Disease: Generalized Thyroid Hormone Resistance
Generalized Thyroid Hormone Resistance 		45 34 7 0.15 2 3.9E-02
CUI: C0026826
Disease: Muscle Hypertonia
Muscle Hypertonia 		197 21 1 4.9E-03 1 2.6E-02
CUI: C1846632
Disease: Thyroid Dyshormonogenesis 6
Thyroid Dyshormonogenesis 6 		1 15 1 0.11 1 3.0E-02
CUI: C3888244
Disease: AICARDI-GOUTIERES SYNDROME 7
AICARDI-GOUTIERES SYNDROME 7 		2 15 1 1.0E-01 1 3.0E-02
CUI: C0271790
Disease: Subclinical hypothyroidism
Subclinical hypothyroidism 		40 10 4 8.9E-02 2 7.4E-02
CUI: C1304508
Disease: Spindle cell hemangioma
Spindle cell hemangioma 		68 10 2 2.7E-02 1 3.6E-02
CUI: C2940786
Disease: Thyroid Hormone Resistance Syndrome
Thyroid Hormone Resistance Syndrome 		25 5 7 0.26 1 4.3E-02
CUI: C0342162
Disease: Compensated hypothyroidism
Compensated hypothyroidism 		7 1 2 0.14 1 5.3E-02
CUI: C1846135
Disease: Autistic features
Autistic features 		3 1 2 0.20 1 5.3E-02
CUI: C2940785
Disease: HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 3
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 3 		8 1 5 0.42 1 5.3E-02
CUI: C0000731
Disease: Abdomen distended
Abdomen distended 		103 0 4 3.7E-02 0 0
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		1098 0 2 1.8E-03 0 0
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		251 0 1 3.9E-03 0 0
CUI: C0001080
Disease: Achondroplasia
Achondroplasia 		46 0 1 1.9E-02 0 0
CUI: C0001206
Disease: Acromegaly
Acromegaly 		138 0 2 1.4E-02 0 0
CUI: C0001311
Disease: Acute bronchiolitis
Acute bronchiolitis 		11 0 1 5.3E-02 0 0
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis 		435 0 1 2.3E-03 0 0
CUI: C0001403
Disease: Addison Disease
Addison Disease 		111 0 2 1.7E-02 0 0