Source: INFERRED ×
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: C2732838
Disease: Neoplasm of skeletal system
Neoplasm of skeletal system 		15 0 1 6.7E-02 0 0
CUI: C0340375
Disease: Subaortic stenosis
Subaortic stenosis 		16 0 1 6.2E-02 0 0
CUI: C0344539
Disease: Hypoplasia of iris
Hypoplasia of iris 		16 0 1 6.2E-02 0 0
CUI: C1840238
Disease: Midnasal stenosis
Midnasal stenosis 		16 0 1 6.2E-02 0 0
CUI: C4021020
Disease: Non-midline cleft lip
Non-midline cleft lip 		16 0 1 6.2E-02 0 0
CUI: C3152182
Disease: Anterior chamber anomalies
Anterior chamber anomalies 		17 0 1 5.9E-02 0 0
CUI: C4021343
Disease: Broad hallux phalanx
Broad hallux phalanx 		17 0 1 5.9E-02 0 0
CUI: C4021977
Disease: Visceral angiomatosis
Visceral angiomatosis 		17 0 1 5.9E-02 0 0
CUI: C0266667
Disease: Cyclocephaly
Cyclocephaly 		18 0 1 5.6E-02 0 0
CUI: C0431362
Disease: Lobar Holoprosencephaly
Lobar Holoprosencephaly 		18 0 1 5.6E-02 0 0
CUI: C1846434
Disease: Hypoplastic scapulae
Hypoplastic scapulae 		18 0 1 5.6E-02 0 0
CUI: C1859775
Disease: Anterior pituitary hypoplasia
Anterior pituitary hypoplasia 		18 0 1 5.6E-02 0 0
CUI: C4022675
Disease: Increased female libido
Increased female libido 		18 0 1 5.6E-02 0 0
CUI: C4025901
Disease: Abnormality of body height
Abnormality of body height 		18 0 1 5.6E-02 0 0
CUI: C0078981
Disease: Arachnoid Cysts
Arachnoid Cysts 		19 0 1 5.3E-02 0 0
CUI: C0338503
Disease: Septo-Optic Dysplasia
Septo-Optic Dysplasia 		19 0 1 5.3E-02 0 0
CUI: C1856266
Disease: Coronal craniosynostosis
Coronal craniosynostosis 		19 0 1 5.3E-02 0 0
CUI: C2936786
Disease: Aqueductal Stenosis
Aqueductal Stenosis 		19 0 1 5.3E-02 0 0
CUI: C1840235
Disease: SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR
SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR 		20 0 1 5.0E-02 0 0
CUI: C1865244
Disease: Shallow orbits
Shallow orbits 		20 0 1 5.0E-02 0 0
CUI: C0004114
Disease: Astrocytoma
Astrocytoma 		21 0 1 4.8E-02 0 0
CUI: C3179508
Disease: Aplasia/Hypoplasia of the thumb
Aplasia/Hypoplasia of the thumb 		21 0 1 4.8E-02 0 0
CUI: C4025569
Disease: Eunuchoid habitus
Eunuchoid habitus 		21 0 1 4.8E-02 0 0
CUI: C0086795
Disease: Pfaundler-Hurler Syndrome
Pfaundler-Hurler Syndrome 		22 0 1 4.5E-02 0 0
CUI: C0242343
Disease: Panhypopituitarism
Panhypopituitarism 		22 0 1 4.5E-02 0 0