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: C1864436
Disease: Muenke Syndrome
Muenke Syndrome
3 0 3 0.75 0 0
CUI: C1450010
Disease: Plagiocephaly, Nonsynostotic
Plagiocephaly, Nonsynostotic
2 0 2 0.50 0 0
Cutis Gyrata Syndrome of Beare And Stevenson
2 0 2 0.50 0 0
CUI: C1863363
Disease: Cartilaginous trachea
Cartilaginous trachea
2 0 2 0.50 0 0
CUI: C2931888
Disease: Pfeiffer type acrocephalosyndactyly
Pfeiffer type acrocephalosyndactyly
2 0 2 0.50 0 0
CUI: C4024730
Disease: Calcaneonavicular fusion
Calcaneonavicular fusion
2 0 2 0.50 0 0
CUI: C4021164
Disease: Bicoronal synostosis
Bicoronal synostosis
6 0 3 0.43 0 0
CUI: C0795998
Disease: JACKSON-WEISS SYNDROME
JACKSON-WEISS SYNDROME
3 0 2 0.40 0 0
CUI: C1863200
Disease: Lacrimal gland hypoplasia
Lacrimal gland hypoplasia
3 0 2 0.40 0 0
CUI: C4021377
Disease: Prominent crus of helix
Prominent crus of helix
3 0 2 0.40 0 0
CUI: C4021418
Disease: Absent proximal phalanx of thumb
Absent proximal phalanx of thumb
3 0 2 0.40 0 0
CUI: C4021564
Disease: Hypoplasia of the lacrimal punctum
Hypoplasia of the lacrimal punctum
3 0 2 0.40 0 0
CUI: C4021627
Disease: Bilateral triphalangeal thumbs
Bilateral triphalangeal thumbs
3 0 2 0.40 0 0
CUI: C4024215
Disease: Aplasia of the parotid gland
Aplasia of the parotid gland
3 0 2 0.40 0 0
CUI: C4024822
Disease: Lacrimal gland aplasia
Lacrimal gland aplasia
3 0 2 0.40 0 0
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome
8 0 3 0.33 0 0
CUI: C0546297
Disease: Hallux Varus
Hallux Varus
4 0 2 0.33 0 0
CUI: C1394030
Disease: Coronal hypospadias
Coronal hypospadias
4 0 2 0.33 0 0
CUI: C1858569
Disease: Absence of Stensen duct
Absence of Stensen duct
4 0 2 0.33 0 0
CUI: C1860050
Disease: Cloverleaf skull
Cloverleaf skull
8 0 3 0.33 0 0
CUI: C1968574
Disease: Hypoplastic lacrimal duct
Hypoplastic lacrimal duct
4 0 2 0.33 0 0
CUI: C4024345
Disease: Radial deviation of the 3rd finger
Radial deviation of the 3rd finger
4 0 2 0.33 0 0
Lacrimoauriculodentodigital syndrome
5 0 2 0.29 0 0
Congenital duodenal obstruction due to malrotation of intestine
5 0 2 0.29 0 0
CUI: C0846967
Disease: Acanthoma
Acanthoma
5 0 2 0.29 0 0