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: C4280681
Disease: Gastrojejunal tube feeding in infancy
Gastrojejunal tube feeding in infancy 		1 0 1 7.1E-02 0 0
CUI: C4479526
Disease: RETINITIS PIGMENTOSA 79
RETINITIS PIGMENTOSA 79 		1 0 1 7.1E-02 0 0
CUI: C4540474
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 51
MENTAL RETARDATION, AUTOSOMAL DOMINANT 51 		1 0 1 7.1E-02 0 0
CUI: C4708498
Disease: PURA syndrome
PURA syndrome 		1 0 1 7.1E-02 0 0
CUI: C0549629
Disease: Abnormal delivery
Abnormal delivery 		32 37 3 7.0E-02 3 7.3E-02
CUI: C0398563
Disease: Deficiency of hexokinase (disorder)
Deficiency of hexokinase (disorder) 		2 0 1 6.7E-02 0 0
CUI: C1740801
Disease: Exaggerated startle response
Exaggerated startle response 		18 4 2 6.7E-02 1 1.0E-01
CUI: C3715199
Disease: RENAL-HEPATIC-PANCREATIC DYSPLASIA 1
RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 		2 0 1 6.7E-02 0 0
CUI: C4021555
Disease: Clinodactyly of the 3rd toe
Clinodactyly of the 3rd toe 		2 0 1 6.7E-02 0 0
CUI: C4023073
Disease: EEG with temporal focal spikes
EEG with temporal focal spikes 		2 0 1 6.7E-02 0 0
CUI: C4553013
Disease: Chemokine (C-C Motif) Ligand 21 Measurement
Chemokine (C-C Motif) Ligand 21 Measurement 		2 0 1 6.7E-02 0 0
CUI: C0079352
Disease: Congenital torticollis
Congenital torticollis 		19 6 2 6.5E-02 2 0.18
CUI: C0231274
Disease: Intolerant of heat
Intolerant of heat 		19 7 2 6.5E-02 1 7.7E-02
CUI: C0018946
Disease: Hematoma, Subdural
Hematoma, Subdural 		3 1 1 6.2E-02 1 0.14
CUI: C0700379
Disease: Total iron binding capacity function
Total iron binding capacity function 		20 0 2 6.2E-02 0 0
CUI: C1283048
Disease: Iron binding capacity total measurement
Iron binding capacity total measurement 		20 0 2 6.2E-02 0 0
CUI: C1837552
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L (disorder)
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L (disorder) 		3 0 1 6.2E-02 0 0
CUI: C2673883
Disease: RENAL-HEPATIC-PANCREATIC DYSPLASIA
RENAL-HEPATIC-PANCREATIC DYSPLASIA 		3 0 1 6.2E-02 0 0
CUI: C3279904
Disease: Lactate Dehydrogenase B Deficiency
Lactate Dehydrogenase B Deficiency 		3 0 1 6.2E-02 0 0
CUI: C4021650
Disease: Short third metatarsal
Short third metatarsal 		3 2 1 6.2E-02 1 0.12
CUI: C4022735
Disease: Cerebral white matter atrophy
Cerebral white matter atrophy 		20 11 2 6.2E-02 1 5.9E-02
CUI: C4024881
Disease: Few cafe-au-lait spots
Few cafe-au-lait spots 		3 2 1 6.2E-02 1 0.12
CUI: C4024943
Disease: Decreased amplitude of sensory action potentials
Decreased amplitude of sensory action potentials 		3 0 1 6.2E-02 0 0
CUI: C1846868
Disease: Parkinsonism with favorable response to dopaminergic medication
Parkinsonism with favorable response to dopaminergic medication 		21 2 2 6.1E-02 2 0.29
CUI: C0524541
Disease: Deciduoma
Deciduoma 		4 0 1 5.9E-02 0 0