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: C0032357
Disease: Poland Syndrome
Poland Syndrome 		1 0 1 1.0E-01 0 0
CUI: C0265425
Disease: 9p partial monosomy syndrome
9p partial monosomy syndrome 		1 0 1 1.0E-01 0 0
CUI: C0543837
Disease: Respiratory distress syndrome, children
Respiratory distress syndrome, children 		1 0 1 1.0E-01 0 0
CUI: C0796182
Disease: Acromelic frontonasal dysplasia
Acromelic frontonasal dysplasia 		1 0 1 1.0E-01 0 0
CUI: C1832352
Disease: Oculoauriculofrontonasal syndrome
Oculoauriculofrontonasal syndrome 		1 0 1 1.0E-01 0 0
CUI: C1844722
Disease: Unilateral breast hypoplasia
Unilateral breast hypoplasia 		1 0 1 1.0E-01 0 0
CUI: C1846266
Disease: Laterally curved eyebrow
Laterally curved eyebrow 		1 0 1 1.0E-01 0 0
CUI: C1850961
Disease: Anterior basal encephalocele
Anterior basal encephalocele 		1 0 1 1.0E-01 0 0
CUI: C1850970
Disease: Frontal cutaneous lipoma
Frontal cutaneous lipoma 		1 0 1 1.0E-01 0 0
CUI: C1863616
Disease: ACROMELIC FRONTONASAL DYSOSTOSIS
ACROMELIC FRONTONASAL DYSOSTOSIS 		1 0 1 1.0E-01 0 0
CUI: C1865044
Disease: PARIETAL FORAMINA 2
PARIETAL FORAMINA 2 		1 0 1 1.0E-01 0 0
CUI: C2675730
Disease: Deafness, Congenital, and Onychodystrophy, Autosomal Dominant
Deafness, Congenital, and Onychodystrophy, Autosomal Dominant 		1 0 1 1.0E-01 0 0
CUI: C2750355
Disease: Omodysplasia 2
Omodysplasia 2 		1 0 1 1.0E-01 0 0
CUI: C2750433
Disease: Bifid Nose With Or Without Anorectal And Renal Anomalies
Bifid Nose With Or Without Anorectal And Renal Anomalies 		1 0 1 1.0E-01 0 0
CUI: C2751431
Disease: Bifid Nose, Autosomal Dominant
Bifid Nose, Autosomal Dominant 		1 0 1 1.0E-01 0 0
CUI: C3150703
Disease: FRONTONASAL DYSPLASIA 2
FRONTONASAL DYSPLASIA 2 		1 0 1 1.0E-01 0 0
CUI: C3280974
Disease: TRIGONOCEPHALY 2
TRIGONOCEPHALY 2 		1 0 1 1.0E-01 0 0
CUI: C3809819
Disease: CRANIOSYNOSTOSIS 5, SUSCEPTIBILITY TO
CRANIOSYNOSTOSIS 5, SUSCEPTIBILITY TO 		1 0 1 1.0E-01 0 0
CUI: C3887497
Disease: Bifid Nose, Autosomal Recessive
Bifid Nose, Autosomal Recessive 		1 0 1 1.0E-01 0 0
CUI: C3888212
Disease: SECKEL SYNDROME 4
SECKEL SYNDROME 4 		1 0 1 1.0E-01 0 0
CUI: C4021030
Disease: Type III lissencephaly
Type III lissencephaly 		1 0 1 1.0E-01 0 0
CUI: C4021292
Disease: Flexion contracture of the 4th toe
Flexion contracture of the 4th toe 		1 0 1 1.0E-01 0 0
CUI: C4021296
Disease: Flexion contracture of the 2nd toe
Flexion contracture of the 2nd toe 		1 0 1 1.0E-01 0 0
CUI: C4021763
Disease: Abnormality of the glabella
Abnormality of the glabella 		1 0 1 1.0E-01 0 0
CUI: C4022992
Disease: Abnormal respiratory system morphology
Abnormal respiratory system morphology 		1 0 1 1.0E-01 0 0