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: C0349398
Disease: Paranoid delusion
Paranoid delusion 		1 0 1 0.50 0 0
CUI: C0432240
Disease: Stuve-Wiedemann dysplasia
Stuve-Wiedemann dysplasia 		1 0 1 0.50 0 0
CUI: C0457928
Disease: Bent bone dysplasia group
Bent bone dysplasia group 		1 0 1 0.50 0 0
CUI: C1832146
Disease: Metaphyseal rarefaction
Metaphyseal rarefaction 		1 0 1 0.50 0 0
CUI: C1835101
Disease: Wide tufts of distal phalanges
Wide tufts of distal phalanges 		1 0 1 0.50 0 0
CUI: C1856778
Disease: Widely patent coronal suture
Widely patent coronal suture 		1 0 1 0.50 0 0
CUI: C1857139
Disease: Abnormal metaphyseal trabeculation
Abnormal metaphyseal trabeculation 		1 0 1 0.50 0 0
CUI: C3278138
Disease: FIBROCHONDROGENESIS 1
FIBROCHONDROGENESIS 1 		1 0 1 0.50 0 0
CUI: C4015965
Disease: MARSHALL/STICKLER SYNDROME
MARSHALL/STICKLER SYNDROME 		1 0 1 0.50 0 0
CUI: C4022181
Disease: Meningeal calcification
Meningeal calcification 		1 0 1 0.50 0 0
CUI: C4022969
Disease: Small proximal tibial epiphyses
Small proximal tibial epiphyses 		1 0 1 0.50 0 0
CUI: C4022970
Disease: Small distal femoral epiphysis
Small distal femoral epiphysis 		1 0 1 0.50 0 0
CUI: C4025045
Disease: Irregular proximal tibial epiphyses
Irregular proximal tibial epiphyses 		1 0 1 0.50 0 0
CUI: C0265235
Disease: Marshall syndrome
Marshall syndrome 		2 0 1 0.33 0 0
CUI: C1504382
Disease: Pulmonary arterial medial hypertrophy
Pulmonary arterial medial hypertrophy 		2 0 1 0.33 0 0
CUI: C1856779
Disease: Widely patent sagittal suture
Widely patent sagittal suture 		2 0 1 0.33 0 0
CUI: C3151066
Disease: RETINITIS PIGMENTOSA 45
RETINITIS PIGMENTOSA 45 		2 0 1 0.33 0 0
CUI: C4014354
Disease: PONTOCEREBELLAR HYPOPLASIA, TYPE 9
PONTOCEREBELLAR HYPOPLASIA, TYPE 9 		2 0 1 0.33 0 0
CUI: C4024831
Disease: Blotching pigmentation of the skin
Blotching pigmentation of the skin 		2 0 1 0.33 0 0
CUI: C4025050
Disease: Irregular distal femoral epiphysis
Irregular distal femoral epiphysis 		2 0 1 0.33 0 0
CUI: C4025356
Disease: Abnormal vitreous humor morphology
Abnormal vitreous humor morphology 		2 0 1 0.33 0 0
CUI: C0155366
Disease: Vitreous degeneration
Vitreous degeneration 		3 0 1 0.25 0 0
CUI: C0155964
Disease: Atrophy of tongue papillae
Atrophy of tongue papillae 		3 0 1 0.25 0 0
CUI: C0265282
Disease: Fibrochondrogenesis
Fibrochondrogenesis 		3 0 1 0.25 0 0
CUI: C1832130
Disease: Pursed lips
Pursed lips 		3 0 1 0.25 0 0