Source: CURATED ×
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: C0206620
Disease: Lymphangioma, Cystic
Lymphangioma, Cystic 		1 0 1 0.33 0 0
CUI: C0240543
Disease: Bulbous nose
Bulbous nose 		1 13 1 0.33 2 3.2E-02
CUI: C0270254
Disease: Hydrops of placenta
Hydrops of placenta 		1 0 1 0.33 0 0
CUI: C0796135
Disease: Renpenning syndrome 1
Renpenning syndrome 1 		1 0 1 0.33 0 0
CUI: C1332140
Disease: Acrofacial Dysostosis
Acrofacial Dysostosis 		1 0 1 0.33 0 0
CUI: C4225317
Disease: ACROFACIAL DYSOSTOSIS, CINCINNATI TYPE
ACROFACIAL DYSOSTOSIS, CINCINNATI TYPE 		1 0 1 0.33 0 0
CUI: C0014804
Disease: Erythromelalgia
Erythromelalgia 		2 0 1 0.25 0 0
CUI: C0031192
Disease: Persistent Ostium Primum
Persistent Ostium Primum 		2 0 1 0.25 0 0
CUI: C0431368
Disease: Partial agenesis of corpus callosum
Partial agenesis of corpus callosum 		2 0 1 0.25 0 0
CUI: C1837822
Disease: Burn-Mckeown syndrome
Burn-Mckeown syndrome 		2 0 1 0.25 0 0
CUI: C0152025
Disease: Polyneuropathy
Polyneuropathy 		4 0 1 0.17 0 0
CUI: C0751603
Disease: Autosomal Recessive Hereditary Spastic Paraplegia
Autosomal Recessive Hereditary Spastic Paraplegia 		4 0 1 0.17 0 0
CUI: C0751604
Disease: Hereditary X-Linked Recessive Spastic Paraplegia
Hereditary X-Linked Recessive Spastic Paraplegia 		4 0 1 0.17 0 0
CUI: C0751605
Disease: X-Linked, Spastic Paraplegia, Hereditary
X-Linked, Spastic Paraplegia, Hereditary 		4 0 1 0.17 0 0
CUI: C4553743
Disease: Spasticity, CTCAE
Spasticity, CTCAE 		4 0 1 0.17 0 0
CUI: C0009917
Disease: Contracture
Contracture 		5 0 1 0.14 0 0
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects 		5 43 1 0.14 2 2.2E-02
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity 		5 39 1 0.14 2 2.2E-02
CUI: C0266470
Disease: Cerebellar Hypoplasia
Cerebellar Hypoplasia 		5 0 1 0.14 0 0
CUI: C0751602
Disease: Hereditary Autosomal Dominant Spastic Paraplegia
Hereditary Autosomal Dominant Spastic Paraplegia 		5 0 1 0.14 0 0
CUI: C4721916
Disease: HMSN Type V
HMSN Type V 		5 0 1 0.14 0 0
CUI: C0020255
Disease: Hydrocephalus
Hydrocephalus 		9 24 1 9.1E-02 3 4.1E-02
CUI: C0344724
Disease: Ostium secundum atrial septal defect
Ostium secundum atrial septal defect 		9 0 1 9.1E-02 0 0
CUI: C0037773
Disease: Spastic Paraplegia, Hereditary
Spastic Paraplegia, Hereditary 		14 0 1 6.2E-02 0 0
CUI: C0020305
Disease: Hydrops Fetalis
Hydrops Fetalis 		19 0 1 4.8E-02 0 0