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: C0264963
Disease: Aneurysm of femoral artery
Aneurysm of femoral artery
1 0 1 0.50 0 0
CUI: C4025413
Disease: Curved fingers
Curved fingers
1 0 1 0.50 0 0
MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED
1 0 1 0.50 0 0
CUI: C4476855
Disease: 5-minute APGAR score of 5
5-minute APGAR score of 5
1 0 1 0.50 0 0
CUI: C4476858
Disease: 1-minute APGAR score of 1
1-minute APGAR score of 1
1 0 1 0.50 0 0
CUI: C4477068
Disease: Abnormality of the periodontium
Abnormality of the periodontium
1 0 1 0.50 0 0
CUI: C4531077
Disease: Abnormal thyroid hormone level
Abnormal thyroid hormone level
1 0 1 0.50 0 0
CUI: C1970777
Disease: Abnormally folded helix
Abnormally folded helix
2 0 1 0.33 0 0
CUI: C3805450
Disease: Calf muscle hypoplasia
Calf muscle hypoplasia
2 0 1 0.33 0 0
CUI: C4524805
Disease: stage IVA gastric cancer
stage IVA gastric cancer
2 0 1 0.33 0 0
CUI: C1622345
Disease: Meretoja syndrome
Meretoja syndrome
3 0 1 0.25 0 0
ARTHROGRYPOSIS, DISTAL, TYPE 4 (disorder)
3 0 1 0.25 0 0
CUI: C1852597
Disease: Arthrogryposis, distal, type 2E
Arthrogryposis, distal, type 2E
3 0 1 0.25 0 0
CUI: C1861238
Disease: ARTHROGRYPOSIS, DISTAL, TYPE 10
ARTHROGRYPOSIS, DISTAL, TYPE 10
3 0 1 0.25 0 0
Arthrogryposis-like hand anomaly and sensorineural deafness
3 0 1 0.25 0 0
CUI: C3554415
Disease: Distal arthrogryposis type 5D
Distal arthrogryposis type 5D
3 0 1 0.25 0 0
CUI: C3806746
Disease: MENTAL RETARDATION, X-LINKED 99
MENTAL RETARDATION, X-LINKED 99
3 0 1 0.25 0 0
CUI: C4016054
Disease: Neonatal Marfan syndrome
Neonatal Marfan syndrome
3 0 1 0.25 0 0
Depigmentation/hyperpigmentation of skin
3 0 1 0.25 0 0
CUI: C4025148
Disease: Hyperextensible thumb
Hyperextensible thumb
3 0 1 0.25 0 0
CUI: C0277005
Disease: Opisthorchis viverrini Infection
Opisthorchis viverrini Infection
4 0 1 0.20 0 0
CUI: C0409354
Disease: Flexion contracture of hip
Flexion contracture of hip
4 0 1 0.20 0 0
CUI: C1862472
Disease: Oculomelic amyoplasia
Oculomelic amyoplasia
4 0 1 0.20 0 0
CUI: C3280526
Disease: ARTHROGRYPOSIS, DISTAL, TYPE 1B
ARTHROGRYPOSIS, DISTAL, TYPE 1B
4 0 1 0.20 0 0
CUI: C4025596
Disease: Abnormality of connective tissue
Abnormality of connective tissue
4 0 1 0.20 0 0