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: C0152438
Disease: Sprengel deformity
Sprengel deformity 		0 4 0 0 1 2.6E-02
CUI: C4703722
Disease: Superior rectus muscle underaction
Superior rectus muscle underaction 		0 1 0 0 1 2.8E-02
CUI: C0025211
Disease: Conjunctival melanosis
Conjunctival melanosis 		1 0 1 0.12 0 0
CUI: C0152091
Disease: Osteochondropathy
Osteochondropathy 		1 0 1 0.12 0 0
CUI: C0243057
Disease: Stomatognathic System Abnormalities
Stomatognathic System Abnormalities 		1 0 1 0.12 0 0
CUI: C0266878
Disease: External resorption of tooth
External resorption of tooth 		1 0 1 0.12 0 0
CUI: C0340639
Disease: Carotid artery aneurysm
Carotid artery aneurysm 		1 0 1 0.12 0 0
CUI: C0432125
Disease: Bicoronal craniosynostosis
Bicoronal craniosynostosis 		1 0 1 0.12 0 0
CUI: C0432149
Disease: Lumbar hemivertebra
Lumbar hemivertebra 		1 0 1 0.12 0 0
CUI: C0432238
Disease: Bent bone dysplasia
Bent bone dysplasia 		1 0 1 0.12 0 0
CUI: C0524686
Disease: Periodontitis, Acute Nonsuppurative
Periodontitis, Acute Nonsuppurative 		1 0 1 0.12 0 0
CUI: C0542142
Disease: Recurrent Laryngeal Nerve Paralysis
Recurrent Laryngeal Nerve Paralysis 		1 0 1 0.12 0 0
CUI: C0685678
Disease: Incomplete ossification of pubis
Incomplete ossification of pubis 		1 0 1 0.12 0 0
CUI: C0686761
Disease: Lack of bone formation
Lack of bone formation 		1 0 1 0.12 0 0
CUI: C1300256
Disease: Thanatophoric dysplasia, type 1
Thanatophoric dysplasia, type 1 		1 4 1 0.12 1 2.6E-02
CUI: C1333286
Disease: Diencephalic Neoplasm
Diencephalic Neoplasm 		1 0 1 0.12 0 0
CUI: C1333987
Disease: Hereditary Glomangioma
Hereditary Glomangioma 		1 0 1 0.12 0 0
CUI: C1334687
Disease: Megakaryocytic Neoplasm
Megakaryocytic Neoplasm 		1 0 1 0.12 0 0
CUI: C1516419
Disease: Cervical Mesonephric Adenocarcinoma
Cervical Mesonephric Adenocarcinoma 		1 0 1 0.12 0 0
CUI: C1516974
Disease: Estrogen Receptor Status - Clinical Trial Eligibility Criteria
Estrogen Receptor Status - Clinical Trial Eligibility Criteria 		1 0 1 0.12 0 0
CUI: C1517658
Disease: Cervical Keratinizing Squamous Cell Carcinoma
Cervical Keratinizing Squamous Cell Carcinoma 		1 0 1 0.12 0 0
CUI: C1834969
Disease: Metaphyseal Dysplasia with Maxillary Hypoplasia and Brachydactyly
Metaphyseal Dysplasia with Maxillary Hypoplasia and Brachydactyly 		1 0 1 0.12 0 0
CUI: C1838416
Disease: CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY
CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY 		1 0 1 0.12 0 0
CUI: C1845146
Disease: Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip-Palate
Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip-Palate 		1 17 1 0.12 1 1.9E-02
CUI: C1851152
Disease: SKELETAL DYSPLASIA WITH ACANTHOSIS NIGRICANS
SKELETAL DYSPLASIA WITH ACANTHOSIS NIGRICANS 		1 0 1 0.12 0 0