Source: INFERRED ×
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: C0337443
Disease: Sodium measurement
Sodium measurement 		0 69 0 0 1 6.3E-03
CUI: C0007113
Disease: Rectal Carcinoma
Rectal Carcinoma 		1 0 1 2.0E-02 0 0
CUI: C0033770
Disease: Prune Belly Syndrome
Prune Belly Syndrome 		1 0 1 2.0E-02 0 0
CUI: C0233283
Disease: Complete breech presentation
Complete breech presentation 		1 0 1 2.0E-02 0 0
CUI: C0271616
Disease: Precocious female puberty
Precocious female puberty 		1 0 1 2.0E-02 0 0
CUI: C0282529
Disease: Chondrodysplasia Punctata, Rhizomelic
Chondrodysplasia Punctata, Rhizomelic 		1 1 1 2.0E-02 1 1.1E-02
CUI: C0338484
Disease: Familial Hemiplegic Migraine
Familial Hemiplegic Migraine 		1 0 1 2.0E-02 0 0
CUI: C0341698
Disease: Atrophy of kidney
Atrophy of kidney 		1 0 1 2.0E-02 0 0
CUI: C0342122
Disease: Toxic diffuse goiter
Toxic diffuse goiter 		1 0 1 2.0E-02 0 0
CUI: C0349450
Disease: Soiling
Soiling 		1 1 1 2.0E-02 1 1.1E-02
CUI: C0598121
Disease: Hypoglycorrhachia
Hypoglycorrhachia 		1 0 1 2.0E-02 0 0
CUI: C1112776
Disease: Thyroid hyperplasia
Thyroid hyperplasia 		1 0 1 2.0E-02 0 0
CUI: C1832466
Disease: CAPOS syndrome
CAPOS syndrome 		1 10 1 2.0E-02 1 1.0E-02
CUI: C1832855
Disease: CHOREOATHETOSIS/SPASTICITY, EPISODIC
CHOREOATHETOSIS/SPASTICITY, EPISODIC 		1 0 1 2.0E-02 0 0
CUI: C1836706
Disease: Hyperthyroidism, Nonautoimmune
Hyperthyroidism, Nonautoimmune 		1 0 1 2.0E-02 0 0
CUI: C1837206
Disease: Cryohydrocytosis, Stomatin-Deficient, with Mental Retardation, Seizures, Cataracts, and Massive Hepatosplenomegaly
Cryohydrocytosis, Stomatin-Deficient, with Mental Retardation, Seizures, Cataracts, and Massive Hepatosplenomegaly 		1 0 1 2.0E-02 0 0
CUI: C1842534
Disease: DYSTONIA 18 (disorder)
DYSTONIA 18 (disorder) 		1 15 1 2.0E-02 1 9.6E-03
CUI: C1842563
Disease: Heterotopia, Periventricular, Autosomal Recessive
Heterotopia, Periventricular, Autosomal Recessive 		1 0 1 2.0E-02 0 0
CUI: C1843140
Disease: SEIZURES, BENIGN FAMILIAL INFANTILE, 3
SEIZURES, BENIGN FAMILIAL INFANTILE, 3 		1 0 1 2.0E-02 0 0
CUI: C1847501
Disease: Glut1 Deficiency Syndrome
Glut1 Deficiency Syndrome 		1 0 1 2.0E-02 0 0
CUI: C1847507
Disease: Paroxysmal lethargy
Paroxysmal lethargy 		1 0 1 2.0E-02 0 0
CUI: C1851734
Disease: Metopic ridge
Metopic ridge 		1 1 1 2.0E-02 1 1.1E-02
CUI: C1855128
Disease: Methylcobalamin Deficiency, CblG Type
Methylcobalamin Deficiency, CblG Type 		1 7 1 2.0E-02 1 1.0E-02
CUI: C1857512
Disease: Temtamy syndrome
Temtamy syndrome 		1 5 1 2.0E-02 1 1.1E-02
CUI: C1863959
Disease: Hyperthyroidism, Familial Gestational
Hyperthyroidism, Familial Gestational 		1 0 1 2.0E-02 0 0