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: C0395905
Disease: Postauricular fistula
Postauricular fistula
1 0 1 0.25 0 0
CUI: C0429803
Disease: Bladder trabeculation
Bladder trabeculation
1 0 1 0.25 0 0
CUI: C0431879
Disease: Brachymesophalangia
Brachymesophalangia
1 0 1 0.25 0 0
MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE
1 0 1 0.25 0 0
CUI: C1862059
Disease: Supraauricular pit
Supraauricular pit
1 0 1 0.25 0 0
CUI: C1862066
Disease: Branchial anomaly
Branchial anomaly
1 0 1 0.25 0 0
CUI: C1862068
Disease: Fusion of middle ear ossicles
Fusion of middle ear ossicles
1 0 1 0.25 0 0
CUI: C2053440
Disease: Thin lower lip vermilion
Thin lower lip vermilion
1 0 1 0.25 0 0
MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1
1 0 1 0.25 0 0
CUI: C4021171
Disease: Prominent tragus
Prominent tragus
1 0 1 0.25 0 0
Prominent superior crus of antihelix
1 0 1 0.25 0 0
CUI: C4021230
Disease: Ectopic lacrimal punctum
Ectopic lacrimal punctum
1 0 1 0.25 0 0
CUI: C4021531
Disease: Hypertrophy of the urinary bladder
Hypertrophy of the urinary bladder
1 0 1 0.25 0 0
CUI: C4022176
Disease: Upper lip pit
Upper lip pit
1 0 1 0.25 0 0
Unilateral conductive hearing impairment
1 0 1 0.25 0 0
CUI: C4023795
Disease: Ectopic thymus tissue
Ectopic thymus tissue
1 0 1 0.25 0 0
CUI: C4293695
Disease: Rectovestibular fistula
Rectovestibular fistula
1 0 1 0.25 0 0
CUI: C4693651
Disease: OROFACIODIGITAL SYNDROME XVIII
OROFACIODIGITAL SYNDROME XVIII
1 0 1 0.25 0 0
CUI: C0265646
Disease: Talipes Calcaneovarus
Talipes Calcaneovarus
2 0 1 0.20 0 0
CUI: C0431697
Disease: Unilateral renal dysplasia
Unilateral renal dysplasia
2 0 1 0.20 0 0
CUI: C1844857
Disease: Short nasal septum
Short nasal septum
2 0 1 0.20 0 0
CUI: C1859223
Disease: Deep longitudinal plantar crease
Deep longitudinal plantar crease
2 0 1 0.20 0 0
CUI: C1867020
Disease: SCALP-EAR-NIPPLE SYNDROME
SCALP-EAR-NIPPLE SYNDROME
2 0 1 0.20 0 0
CUI: C1868570
Disease: CHAR SYNDROME
CHAR SYNDROME
2 0 1 0.20 0 0
CUI: C4021746
Disease: Abnormality of the ilium
Abnormality of the ilium
2 0 1 0.20 0 0