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: C0266677
Disease: Synotus
Synotus 		2 0 2 0.50 0 0
CUI: C1876185
Disease: Dysgnathia complex
Dysgnathia complex 		3 0 2 0.40 0 0
CUI: C0265242
Disease: Otocephaly
Otocephaly 		4 0 2 0.33 0 0
CUI: C0685775
Disease: Congenital absence of jaw
Congenital absence of jaw 		5 0 2 0.29 0 0
CUI: C0276161
Disease: Subacute adenoviral encephalitis
Subacute adenoviral encephalitis 		1 0 1 0.25 0 0
CUI: C1835465
Disease: Short stature, postnatal
Short stature, postnatal 		1 0 1 0.25 0 0
CUI: C1839125
Disease: Say Meyer syndrome
Say Meyer syndrome 		1 0 1 0.25 0 0
CUI: C1864690
Disease: Microphthalmia, Syndromic 5
Microphthalmia, Syndromic 5 		1 0 1 0.25 0 0
CUI: C2678046
Disease: Mental Retardation, X-Linked, Syndromic, Turner Type
Mental Retardation, X-Linked, Syndromic, Turner Type 		1 0 1 0.25 0 0
CUI: C3151440
Disease: PITUITARY HORMONE DEFICIENCY, COMBINED, 6
PITUITARY HORMONE DEFICIENCY, COMBINED, 6 		1 0 1 0.25 0 0
CUI: C3494423
Disease: Maxillary Retroposition
Maxillary Retroposition 		1 0 1 0.25 0 0
CUI: C3494424
Disease: Maxillary Retrusion
Maxillary Retrusion 		1 0 1 0.25 0 0
CUI: C3494425
Disease: Mandibular Retroposition
Mandibular Retroposition 		1 0 1 0.25 0 0
CUI: C3494426
Disease: Mandibular Retrusion
Mandibular Retrusion 		1 0 1 0.25 0 0
CUI: C3804969
Disease: Dysgnathia
Dysgnathia 		1 0 1 0.25 0 0
CUI: C4021811
Disease: Abnormality of the midface
Abnormality of the midface 		1 0 1 0.25 0 0
CUI: C4305151
Disease: Syndromic microphthalmia type 5
Syndromic microphthalmia type 5 		1 0 1 0.25 0 0
CUI: C0265740
Disease: Arrhinia
Arrhinia 		2 0 1 0.20 0 0
CUI: C3151380
Disease: SCHIZOPHRENIA 15
SCHIZOPHRENIA 15 		2 0 1 0.20 0 0
CUI: C4024159
Disease: Aplasia/Hypoplasia involving the nose
Aplasia/Hypoplasia involving the nose 		8 0 2 0.20 0 0
CUI: C4025870
Disease: Abnormality of the mandible
Abnormality of the mandible 		2 0 1 0.20 0 0
CUI: C0035353
Disease: Congenital retrognathism
Congenital retrognathism 		3 0 1 0.17 0 0
CUI: C0158663
Disease: Tongue absent
Tongue absent 		3 0 1 0.17 0 0
CUI: C0410192
Disease: Muscular Dystrophy, Scapulohumeral
Muscular Dystrophy, Scapulohumeral 		3 0 1 0.17 0 0
CUI: C0432442
Disease: Chromosome 18p deletion syndrome
Chromosome 18p deletion syndrome 		3 0 1 0.17 0 0