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: C1856136
Disease: Conical incisor
Conical incisor
10 0 3 0.11 0 0
CUI: C1865244
Disease: Shallow orbits
Shallow orbits
20 0 4 0.11 0 0
CUI: C2930865
Disease: Ramer Ladda syndrome
Ramer Ladda syndrome
10 0 3 0.11 0 0
CUI: C0265535
Disease: Trigonocephaly
Trigonocephaly
52 0 7 0.11 0 0
CUI: C1865847
Disease: Ulnar bowing
Ulnar bowing
12 0 3 0.10 0 0
CUI: C1450010
Disease: Plagiocephaly, Nonsynostotic
Plagiocephaly, Nonsynostotic
2 0 2 1.0E-01 0 0
CUI: C1849227
Disease: Cleft of chin
Cleft of chin
2 0 2 1.0E-01 0 0
Cutis Gyrata Syndrome of Beare And Stevenson
2 16 2 1.0E-01 2 0.12
CUI: C1860048
Disease: Temporal bossing
Temporal bossing
2 0 2 1.0E-01 0 0
CUI: C1863363
Disease: Cartilaginous trachea
Cartilaginous trachea
2 0 2 1.0E-01 0 0
CUI: C1863382
Disease: Absent first metatarsal
Absent first metatarsal
2 0 2 1.0E-01 0 0
CUI: C1863389
Disease: Apert-Crouzon Disease
Apert-Crouzon Disease
2 0 2 1.0E-01 0 0
CUI: C2350233
Disease: Antley-Bixler Syndrome Phenotype
Antley-Bixler Syndrome Phenotype
2 0 2 1.0E-01 0 0
CUI: C2931888
Disease: Pfeiffer type acrocephalosyndactyly
Pfeiffer type acrocephalosyndactyly
2 0 2 1.0E-01 0 0
Partial duplication of the distal phalanx of the 3rd finger
2 0 2 1.0E-01 0 0
Partial duplication of the distal phalanx of the 2nd finger
2 0 2 1.0E-01 0 0
CUI: C4024730
Disease: Calcaneonavicular fusion
Calcaneonavicular fusion
2 0 2 1.0E-01 0 0
CUI: C0010273
Disease: Craniofacial Dysostosis
Craniofacial Dysostosis
14 29 3 9.7E-02 1 3.2E-02
CUI: C4023383
Disease: Narrow internal auditory canal
Narrow internal auditory canal
14 0 3 9.7E-02 0 0
CUI: C0265308
Disease: Baller-Gerold syndrome
Baller-Gerold syndrome
3 0 2 9.5E-02 0 0
CUI: C0795998
Disease: JACKSON-WEISS SYNDROME
JACKSON-WEISS SYNDROME
3 0 2 9.5E-02 0 0
CUI: C1510455
Disease: Acrocephalosyndactylia
Acrocephalosyndactylia
3 0 2 9.5E-02 0 0
CUI: C1862178
Disease: Cole Carpenter syndrome
Cole Carpenter syndrome
3 0 2 9.5E-02 0 0
CUI: C1863200
Disease: Lacrimal gland hypoplasia
Lacrimal gland hypoplasia
3 0 2 9.5E-02 0 0
CUI: C4021418
Disease: Absent proximal phalanx of thumb
Absent proximal phalanx of thumb
3 0 2 9.5E-02 0 0