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: C1847604
Disease: Van der Woude syndrome 2
Van der Woude syndrome 2
2 0 2 0.67 0 0
CUI: C4551864
Disease: VAN DER WOUDE SYNDROME 1
VAN DER WOUDE SYNDROME 1
2 0 2 0.67 0 0
CUI: C1861544
Disease: Lower lip pit
Lower lip pit
3 0 2 0.50 0 0
CUI: C0266092
Disease: Congenital lip pits
Congenital lip pits
4 0 2 0.40 0 0
CUI: C0149772
Disease: Abnormal salivary gland morphology
Abnormal salivary gland morphology
5 0 2 0.33 0 0
CUI: C0158651
Disease: Cleft lip, unilateral, complete
Cleft lip, unilateral, complete
1 0 1 0.33 0 0
OROFACIAL CLEFT 6, SUSCEPTIBILITY TO
1 0 1 0.33 0 0
Nemaline Myopathy 3, With Intranuclear Rods
1 0 1 0.33 0 0
Myopathy, Actin, Congenital, With Cores
1 0 1 0.33 0 0
CUI: C3841283
Disease: Cleft Palate alone
Cleft Palate alone
1 0 1 0.33 0 0
Primary papillary adenocarcinoma of lung
1 0 1 0.33 0 0
CUI: C4021392
Disease: Fibrous syngnathia
Fibrous syngnathia
1 0 1 0.33 0 0
Pyramidal skinfold extending from the base to the top of the nails
1 0 1 0.33 0 0
CUI: C4225181
Disease: MYOPATHY, SCAPULOHUMEROPERONEAL
MYOPATHY, SCAPULOHUMEROPERONEAL
1 0 1 0.33 0 0
CUI: C0231666
Disease: Wrist-Drop
Wrist-Drop
2 0 1 0.25 0 0
CUI: C1335325
Disease: Papillary Lung Adenocarcinoma
Papillary Lung Adenocarcinoma
2 0 1 0.25 0 0
CUI: C3711377
Disease: Intranuclear Rod Myopathy
Intranuclear Rod Myopathy
2 0 1 0.25 0 0
CUI: C3711389
Disease: Actin-Accumulation Myopathy
Actin-Accumulation Myopathy
2 48 1 0.25 1 2.1E-02
CUI: C3810471
Disease: Intercrural pterygium
Intercrural pterygium
2 0 1 0.25 0 0
CUI: C0032805
Disease: Postpericardiotomy Syndrome
Postpericardiotomy Syndrome
3 0 1 0.20 0 0
CUI: C0266122
Disease: Cleft uvula
Cleft uvula
3 0 1 0.20 0 0
CUI: C0270992
Disease: Secondary myopathy
Secondary myopathy
3 0 1 0.20 0 0
CUI: C0376524
Disease: Branchio-Oculo-Facial Syndrome
Branchio-Oculo-Facial Syndrome
9 0 2 0.20 0 0
CUI: C2931268
Disease: Scapuloperoneal myopathy
Scapuloperoneal myopathy
3 0 1 0.20 0 0
CUI: C3150891
Disease: COCOON SYNDROME
COCOON SYNDROME
3 0 1 0.20 0 0