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: C1450010
Disease: Plagiocephaly, Nonsynostotic
Plagiocephaly, Nonsynostotic 		2 0 1 0.50 0 0
CUI: C1849227
Disease: Cleft of chin
Cleft of chin 		2 0 1 0.50 0 0
CUI: C1851797
Disease: Palmoplantar cutis gyrata
Palmoplantar cutis gyrata 		2 0 1 0.50 0 0
CUI: C1852406
Disease: Cutis Gyrata Syndrome of Beare And Stevenson
Cutis Gyrata Syndrome of Beare And Stevenson 		2 16 1 0.50 8 0.47
CUI: C1863363
Disease: Cartilaginous trachea
Cartilaginous trachea 		2 0 1 0.50 0 0
CUI: C1863382
Disease: Absent first metatarsal
Absent first metatarsal 		2 0 1 0.50 0 0
CUI: C1863389
Disease: Apert-Crouzon Disease
Apert-Crouzon Disease 		2 0 1 0.50 0 0
CUI: C1863406
Disease: Anomalous tracheal cartilage
Anomalous tracheal cartilage 		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: C3150931
Disease: Steep acetabular roof
Steep acetabular roof 		2 0 1 0.50 0 0
CUI: C3872820
Disease: Congenital pulmonary acinar dysplasia
Congenital pulmonary acinar dysplasia 		2 0 1 0.50 0 0
CUI: C4021360
Disease: Partial duplication of the distal phalanx of the 3rd finger
Partial duplication of the distal phalanx of the 3rd finger 		2 0 1 0.50 0 0
CUI: C4021365
Disease: Partial duplication of the distal phalanx of the 2nd finger
Partial duplication of the distal phalanx of the 2nd finger 		2 0 1 0.50 0 0
CUI: C4023458
Disease: Abnormal shape of the frontal region
Abnormal shape of the frontal region 		2 0 1 0.50 0 0
CUI: C4024730
Disease: Calcaneonavicular fusion
Calcaneonavicular fusion 		2 0 1 0.50 0 0
CUI: C4025301
Disease: Cervical C5/C6 vertebrae fusion
Cervical C5/C6 vertebrae fusion 		2 0 1 0.50 0 0
CUI: C0687154
Disease: Acrocephalopolysyndactyly
Acrocephalopolysyndactyly 		3 0 1 0.33 0 0
CUI: C0795998
Disease: JACKSON-WEISS SYNDROME
JACKSON-WEISS SYNDROME 		3 20 1 0.33 8 0.38
CUI: C1510455
Disease: Acrocephalosyndactylia
Acrocephalosyndactylia 		3 1 1 0.33 1 0.11
CUI: C1863200
Disease: Lacrimal gland hypoplasia
Lacrimal gland hypoplasia 		3 0 1 0.33 0 0
CUI: C1864436
Disease: Muenke Syndrome
Muenke Syndrome 		3 11 1 0.33 1 5.3E-02
CUI: C3281247
Disease: BENT BONE DYSPLASIA SYNDROME
BENT BONE DYSPLASIA SYNDROME 		3 10 1 0.33 8 0.73
CUI: C3850155
Disease: Congenital Microtia
Congenital Microtia 		3 0 1 0.33 0 0
CUI: C4021377
Disease: Prominent crus of helix
Prominent crus of helix 		3 0 1 0.33 0 0