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: C0524730
Disease: Odontome
Odontome 		10 0 10 1.00 0 0
CUI: C3714873
Disease: Axenfeld-Rieger Syndrome, Type 1
Axenfeld-Rieger Syndrome, Type 1 		4 0 2 0.17 0 0
CUI: C4310809
Disease: ANTERIOR SEGMENT DYSGENESIS 5
ANTERIOR SEGMENT DYSGENESIS 5 		4 0 2 0.17 0 0
CUI: C0344559
Disease: Irido-corneo-trabecular dysgenesis (disorder)
Irido-corneo-trabecular dysgenesis (disorder) 		7 0 2 0.13 0 0
CUI: C0003090
Disease: Ankylosis
Ankylosis 		1 0 1 1.0E-01 0 0
CUI: C0010273
Disease: Craniofacial Dysostosis
Craniofacial Dysostosis 		1 0 1 1.0E-01 0 0
CUI: C0029132
Disease: Disorder of the optic nerve
Disorder of the optic nerve 		1 0 1 1.0E-01 0 0
CUI: C0152112
Disease: Foster-Kennedy Syndrome
Foster-Kennedy Syndrome 		1 0 1 1.0E-01 0 0
CUI: C0243057
Disease: Stomatognathic System Abnormalities
Stomatognathic System Abnormalities 		1 0 1 1.0E-01 0 0
CUI: C0406716
Disease: Hypodontia and nail dysgenesis
Hypodontia and nail dysgenesis 		1 0 1 1.0E-01 0 0
CUI: C0406735
Disease: Hypoplastic enamel-onycholysis-hypohidrosis syndrome
Hypoplastic enamel-onycholysis-hypohidrosis syndrome 		1 0 1 1.0E-01 0 0
CUI: C0549307
Disease: Morning glory syndrome
Morning glory syndrome 		1 0 1 1.0E-01 0 0
CUI: C0751402
Disease: Optic Disk Disorders
Optic Disk Disorders 		1 0 1 1.0E-01 0 0
CUI: C0856830
Disease: Calcium pyrophosphate arthropathy
Calcium pyrophosphate arthropathy 		1 0 1 1.0E-01 0 0
CUI: C0949690
Disease: Spondylarthritis
Spondylarthritis 		1 0 1 1.0E-01 0 0
CUI: C1450010
Disease: Plagiocephaly, Nonsynostotic
Plagiocephaly, Nonsynostotic 		1 0 1 1.0E-01 0 0
CUI: C1833797
Disease: Optic Nerve Hypoplasia, Bilateral
Optic Nerve Hypoplasia, Bilateral 		1 0 1 1.0E-01 0 0
CUI: C1834969
Disease: Metaphyseal Dysplasia with Maxillary Hypoplasia and Brachydactyly
Metaphyseal Dysplasia with Maxillary Hypoplasia and Brachydactyly 		1 0 1 1.0E-01 0 0
CUI: C1835698
Disease: Keratitis, hereditary
Keratitis, hereditary 		1 0 1 1.0E-01 0 0
CUI: C1842031
Disease: IRIDOGONIODYSGENESIS, TYPE 2
IRIDOGONIODYSGENESIS, TYPE 2 		1 0 1 1.0E-01 0 0
CUI: C1852502
Disease: CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT
CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT 		1 0 1 1.0E-01 0 0
CUI: C1859252
Disease: Cerebrofaciothoracic Dysplasia
Cerebrofaciothoracic Dysplasia 		1 0 1 1.0E-01 0 0
CUI: C1865070
Disease: SCAPHOCEPHALY, MAXILLARY RETRUSION, AND MENTAL RETARDATION
SCAPHOCEPHALY, MAXILLARY RETRUSION, AND MENTAL RETARDATION 		1 0 1 1.0E-01 0 0
CUI: C1866507
Disease: Spondyloepimetaphyseal Dysplasia With Abnormal Dentition
Spondyloepimetaphyseal Dysplasia With Abnormal Dentition 		1 0 1 1.0E-01 0 0
CUI: C1866994
Disease: Ulnar-mammary syndrome
Ulnar-mammary syndrome 		1 0 1 1.0E-01 0 0