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: C1840598
Disease: FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 2
FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 2 		0 1 0 0 1 6.3E-04
CUI: C1842247
Disease: CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1 		0 34 0 0 1 6.1E-04
CUI: C4050627
Disease: Soluble P-Selectin Measurement
Soluble P-Selectin Measurement 		0 3 0 0 1 6.2E-04
CUI: C4529962
Disease: Fatty Liver Disease
Fatty Liver Disease 		0 43 0 0 1 6.1E-04
CUI: C1845977
Disease: X- linked recessive
X- linked recessive 		172 0 1 1.1E-03 0 0
CUI: C0231712
Disease: Waddling gait
Waddling gait 		107 0 1 1.2E-03 0 0
CUI: C0022578
Disease: Keratoconus
Keratoconus 		106 0 1 1.2E-03 0 0
CUI: C1844704
Disease: Platyspondyly
Platyspondyly 		93 0 1 1.2E-03 0 0
CUI: C0424230
Disease: Motor retardation
Motor retardation 		92 0 1 1.2E-03 0 0
CUI: C1837249
Disease: Malformations of Cortical Development, Group II
Malformations of Cortical Development, Group II 		92 0 1 1.2E-03 0 0
CUI: C4024818
Disease: Progressive night blindness
Progressive night blindness 		87 0 1 1.2E-03 0 0
CUI: C3806467
Disease: Respiratory insufficiency due to muscle weakness
Respiratory insufficiency due to muscle weakness 		85 0 1 1.2E-03 0 0
CUI: C4551570
Disease: 2-3 toe syndactyly
2-3 toe syndactyly 		85 0 1 1.2E-03 0 0
CUI: C1849340
Disease: Long palpebral fissure
Long palpebral fissure 		73 0 1 1.3E-03 0 0
CUI: C0234533
Disease: Generalized seizures
Generalized seizures 		72 0 1 1.3E-03 0 0
CUI: C0431380
Disease: Cortical Dysplasia
Cortical Dysplasia 		71 0 1 1.3E-03 0 0
CUI: C0085271
Disease: Self-Injurious Behavior
Self-Injurious Behavior 		67 0 1 1.3E-03 0 0
CUI: C1847879
Disease: X-linked dominant inheritance
X-linked dominant inheritance 		65 0 1 1.3E-03 0 0
CUI: C0013363
Disease: Dysautonomia
Dysautonomia 		62 0 1 1.3E-03 0 0
CUI: C0694550
Disease: Recurrent pneumonia
Recurrent pneumonia 		62 0 1 1.3E-03 0 0
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele 		62 0 1 1.3E-03 0 0
CUI: C0853087
Disease: Nail abnormality
Nail abnormality 		61 0 1 1.3E-03 0 0
CUI: C0263523
Disease: Micronychia (disorder)
Micronychia (disorder) 		60 0 1 1.3E-03 0 0
CUI: C0009024
Disease: Clonus
Clonus 		59 0 1 1.3E-03 0 0
CUI: C0232744
Disease: Decreased liver function
Decreased liver function 		59 0 1 1.3E-03 0 0