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: C1876185
Disease: Dysgnathia complex
Dysgnathia complex 		3 0 2 0.67 0 0
CUI: C0265242
Disease: Otocephaly
Otocephaly 		4 0 2 0.50 0 0
CUI: C0276161
Disease: Subacute adenoviral encephalitis
Subacute adenoviral encephalitis 		1 0 1 0.50 0 0
CUI: C1864690
Disease: Microphthalmia, Syndromic 5
Microphthalmia, Syndromic 5 		1 0 1 0.50 0 0
CUI: C3151440
Disease: PITUITARY HORMONE DEFICIENCY, COMBINED, 6
PITUITARY HORMONE DEFICIENCY, COMBINED, 6 		1 0 1 0.50 0 0
CUI: C3494423
Disease: Maxillary Retroposition
Maxillary Retroposition 		1 0 1 0.50 0 0
CUI: C3494424
Disease: Maxillary Retrusion
Maxillary Retrusion 		1 0 1 0.50 0 0
CUI: C3494425
Disease: Mandibular Retroposition
Mandibular Retroposition 		1 0 1 0.50 0 0
CUI: C3494426
Disease: Mandibular Retrusion
Mandibular Retrusion 		1 0 1 0.50 0 0
CUI: C3804969
Disease: Dysgnathia
Dysgnathia 		1 0 1 0.50 0 0
CUI: C4020963
Disease: Absent nares
Absent nares 		4 0 2 0.50 0 0
CUI: C4305151
Disease: Syndromic microphthalmia type 5
Syndromic microphthalmia type 5 		1 0 1 0.50 0 0
CUI: C0685775
Disease: Congenital absence of jaw
Congenital absence of jaw 		5 0 2 0.40 0 0
CUI: C3151380
Disease: SCHIZOPHRENIA 15
SCHIZOPHRENIA 15 		2 0 1 0.33 0 0
CUI: C0035353
Disease: Congenital retrognathism
Congenital retrognathism 		3 0 1 0.25 0 0
CUI: C0158663
Disease: Tongue absent
Tongue absent 		3 0 1 0.25 0 0
CUI: C1395317
Disease: Dextrocardia with situs inversus
Dextrocardia with situs inversus 		3 0 1 0.25 0 0
CUI: C4024159
Disease: Aplasia/Hypoplasia involving the nose
Aplasia/Hypoplasia involving the nose 		8 0 2 0.25 0 0
CUI: C1833798
Disease: Optic Nerve Aplasia, Bilateral
Optic Nerve Aplasia, Bilateral 		4 0 1 0.20 0 0
CUI: C1864871
Disease: Chromosome 17q21.31 Deletion Syndrome
Chromosome 17q21.31 Deletion Syndrome 		4 0 1 0.20 0 0
CUI: C1865295
Disease: Auriculo-condylar syndrome
Auriculo-condylar syndrome 		4 0 1 0.20 0 0
CUI: C1396772
Disease: Hypoplasia of the epiglottis
Hypoplasia of the epiglottis 		5 0 1 0.17 0 0
CUI: C1859773
Disease: Microphthalmia, Syndromic 3
Microphthalmia, Syndromic 3 		5 0 1 0.17 0 0
CUI: C0265245
Disease: Nager syndrome
Nager syndrome 		6 0 1 0.14 0 0
CUI: C0685776
Disease: Congenital absence of mandible
Congenital absence of mandible 		14 0 2 0.14 0 0