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: C0004106
Disease: Astigmatism
Astigmatism
0 45 0 0 2 2.1E-02
CUI: C0152438
Disease: Sprengel deformity
Sprengel deformity
0 4 0 0 1 1.8E-02
CUI: C4703722
Disease: Superior rectus muscle underaction
Superior rectus muscle underaction
0 1 0 0 1 1.9E-02
CUI: C0025211
Disease: Conjunctival melanosis
Conjunctival melanosis
1 0 1 6.7E-02 0 0
CUI: C0152091
Disease: Osteochondropathy
Osteochondropathy
1 0 1 6.7E-02 0 0
CUI: C0264402
Disease: Gas bubble disease
Gas bubble disease
1 0 1 6.7E-02 0 0
CUI: C0265241
Disease: Franceschetti-Klein syndrome
Franceschetti-Klein syndrome
1 0 1 6.7E-02 0 0
CUI: C0340639
Disease: Carotid artery aneurysm
Carotid artery aneurysm
1 0 1 6.7E-02 0 0
CUI: C0432125
Disease: Bicoronal craniosynostosis
Bicoronal craniosynostosis
1 0 1 6.7E-02 0 0
CUI: C0432149
Disease: Lumbar hemivertebra
Lumbar hemivertebra
1 0 1 6.7E-02 0 0
CUI: C0432238
Disease: Bent bone dysplasia
Bent bone dysplasia
1 0 1 6.7E-02 0 0
CUI: C0524686
Disease: Periodontitis, Acute Nonsuppurative
Periodontitis, Acute Nonsuppurative
1 0 1 6.7E-02 0 0
CUI: C0542142
Disease: Recurrent Laryngeal Nerve Paralysis
Recurrent Laryngeal Nerve Paralysis
1 0 1 6.7E-02 0 0
CUI: C0685678
Disease: Incomplete ossification of pubis
Incomplete ossification of pubis
1 0 1 6.7E-02 0 0
Arnold-Chiari Malformation, Type III
1 0 1 6.7E-02 0 0
CUI: C0750932
Disease: Arnold-Chiari Malformation, Type IV
Arnold-Chiari Malformation, Type IV
1 0 1 6.7E-02 0 0
CUI: C1300256
Disease: Thanatophoric dysplasia, type 1
Thanatophoric dysplasia, type 1
1 4 1 6.7E-02 1 1.8E-02
CUI: C1333286
Disease: Diencephalic Neoplasm
Diencephalic Neoplasm
1 0 1 6.7E-02 0 0
CUI: C1333987
Disease: Hereditary Glomangioma
Hereditary Glomangioma
1 0 1 6.7E-02 0 0
CUI: C1334687
Disease: Megakaryocytic Neoplasm
Megakaryocytic Neoplasm
1 0 1 6.7E-02 0 0
CUI: C1516419
Disease: Cervical Mesonephric Adenocarcinoma
Cervical Mesonephric Adenocarcinoma
1 0 1 6.7E-02 0 0
Estrogen Receptor Status - Clinical Trial Eligibility Criteria
1 0 1 6.7E-02 0 0
Cervical Keratinizing Squamous Cell Carcinoma
1 0 1 6.7E-02 0 0
Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip-Palate
1 0 1 6.7E-02 0 0
CUI: C1848108
Disease: Long ulna
Long ulna
1 0 1 6.7E-02 0 0