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: C0742794
Disease: Multiple contractures
Multiple contractures 		1 0 1 0.50 0 0
CUI: C3809845
Disease: EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2
EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2 		1 0 1 0.50 0 0
CUI: C4303787
Disease: Ehlers-Danlos syndrome musculocontractural type
Ehlers-Danlos syndrome musculocontractural type 		1 0 1 0.50 0 0
CUI: C1833136
Disease: Marden Walker like syndrome
Marden Walker like syndrome 		2 0 1 0.33 0 0
CUI: C4025716
Disease: Abnormality of the duodenum
Abnormality of the duodenum 		2 0 1 0.33 0 0
CUI: C4551497
Disease: Ehlers-Danlos syndrome kyphoscoliotic type
Ehlers-Danlos syndrome kyphoscoliotic type 		2 0 1 0.33 0 0
CUI: C0022410
Disease: Joint Instability
Joint Instability 		3 0 1 0.25 0 0
CUI: C0431886
Disease: Thumb in palm deformity
Thumb in palm deformity 		3 0 1 0.25 0 0
CUI: C0427201
Disease: Floppy Muscles
Floppy Muscles 		6 0 1 0.14 0 0
CUI: C0427202
Disease: Muscle Tone Atonic
Muscle Tone Atonic 		6 0 1 0.14 0 0
CUI: C0238577
Disease: Abdominal wall defect
Abdominal wall defect 		8 0 1 0.11 0 0
CUI: C0751330
Disease: Unilateral Hypotonia
Unilateral Hypotonia 		8 0 1 0.11 0 0
CUI: C0796033
Disease: MARDEN-WALKER SYNDROME
MARDEN-WALKER SYNDROME 		8 0 1 0.11 0 0
CUI: C1857485
Disease: Flat forehead
Flat forehead 		11 0 1 8.3E-02 0 0
CUI: C0008767
Disease: Cicatrization
Cicatrization 		13 0 1 7.1E-02 0 0
CUI: C0678909
Disease: Brain Waves
Brain Waves 		14 0 1 6.7E-02 0 0
CUI: C0026825
Disease: Flaccid Muscle Tone
Flaccid Muscle Tone 		16 0 1 5.9E-02 0 0
CUI: C1291314
Disease: Deficiency of monooxygenase
Deficiency of monooxygenase 		17 0 1 5.6E-02 0 0
CUI: C3152182
Disease: Anterior chamber anomalies
Anterior chamber anomalies 		18 0 1 5.3E-02 0 0
CUI: C0221766
Disease: Diastasis recti
Diastasis recti 		22 0 1 4.3E-02 0 0
CUI: C0265213
Disease: Distal arthrogryposis syndrome
Distal arthrogryposis syndrome 		22 0 1 4.3E-02 0 0
CUI: C0026633
Disease: Mouth Abnormalities
Mouth Abnormalities 		26 0 1 3.7E-02 0 0
CUI: C0241181
Disease: Fragile skin
Fragile skin 		26 0 1 3.7E-02 0 0
CUI: C1845251
Disease: Facial hypotonia
Facial hypotonia 		33 0 1 2.9E-02 0 0
CUI: C0542514
Disease: Blue sclera
Blue sclera 		70 0 2 2.9E-02 0 0