Source: CURATED ×
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: C0003090
Disease: Ankylosis
Ankylosis 		1 0 1 1.00 0 0
CUI: C0010273
Disease: Craniofacial Dysostosis
Craniofacial Dysostosis 		1 0 1 1.00 0 0
CUI: C1450010
Disease: Plagiocephaly, Nonsynostotic
Plagiocephaly, Nonsynostotic 		1 0 1 1.00 0 0
CUI: C1867564
Disease: SCAPHOCEPHALY AND AXENFELD-RIEGER ANOMALY
SCAPHOCEPHALY AND AXENFELD-RIEGER ANOMALY 		1 1 1 1.00 1 0.11
CUI: C3267076
Disease: Familial scaphocephaly syndrome
Familial scaphocephaly syndrome 		1 0 1 1.00 0 0
CUI: C3281247
Disease: BENT BONE DYSPLASIA SYNDROME
BENT BONE DYSPLASIA SYNDROME 		1 10 1 1.00 8 0.73
CUI: C0001193
Disease: Apert syndrome
Apert syndrome 		2 14 1 0.50 8 0.53
CUI: C0265326
Disease: Bannayan-Riley-Ruvalcaba Syndrome
Bannayan-Riley-Ruvalcaba Syndrome 		2 0 1 0.50 0 0
CUI: C0391826
Disease: Lhermitte-Duclos disease
Lhermitte-Duclos disease 		2 0 1 0.50 0 0
CUI: C0795998
Disease: JACKSON-WEISS SYNDROME
JACKSON-WEISS SYNDROME 		2 15 1 0.50 8 0.50
CUI: C1510455
Disease: Acrocephalosyndactylia
Acrocephalosyndactylia 		2 1 1 0.50 1 0.11
CUI: C1852406
Disease: Cutis Gyrata Syndrome of Beare And Stevenson
Cutis Gyrata Syndrome of Beare And Stevenson 		2 13 1 0.50 8 0.57
CUI: C1860042
Disease: Antley-Bixler Syndrome with Disordered Steroidogenesis
Antley-Bixler Syndrome with Disordered Steroidogenesis 		2 0 1 0.50 0 0
CUI: C1863389
Disease: Apert-Crouzon Disease
Apert-Crouzon Disease 		2 0 1 0.50 0 0
CUI: C1959582
Disease: PTEN Hamartoma Tumor Syndrome
PTEN Hamartoma Tumor Syndrome 		2 0 1 0.50 0 0
CUI: C2350233
Disease: Antley-Bixler Syndrome Phenotype
Antley-Bixler Syndrome Phenotype 		2 0 1 0.50 0 0
CUI: C2931888
Disease: Pfeiffer type acrocephalosyndactyly
Pfeiffer type acrocephalosyndactyly 		2 0 1 0.50 0 0
CUI: C2936791
Disease: Antley-Bixler Syndrome, Autosomal Dominant
Antley-Bixler Syndrome, Autosomal Dominant 		2 10 1 0.50 8 0.73
CUI: C0175699
Disease: Saethre-Chotzen Syndrome
Saethre-Chotzen Syndrome 		3 29 1 0.33 8 0.27
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		3 31 1 0.33 8 0.25
CUI: C0265269
Disease: Lacrimoauriculodentodigital syndrome
Lacrimoauriculodentodigital syndrome 		3 32 1 0.33 8 0.24
CUI: C0685381
Disease: Congenital hypoplasia of radius
Congenital hypoplasia of radius 		3 0 1 0.33 0 0
CUI: C2931196
Disease: Craniofacial dysostosis type 1
Craniofacial dysostosis type 1 		3 38 1 0.33 9 0.24
CUI: C1153706
Disease: Endometrial adenocarcinoma
Endometrial adenocarcinoma 		4 0 1 0.25 0 0
CUI: C0011757
Disease: Developmental Coordination Disorder
Developmental Coordination Disorder 		8 0 1 0.12 0 0