Disease #05209 (ODA (Ocular developmental anomalies))

Official abbreviation ODA
Name Ocular developmental anomalies
OMIM ID -
Inheritance -
Individuals reported having this disease 7
Phenotype entries for this disease 7
Associated with 1 gene PTCH1
Associated tissues eyes
Disease features Anophthalmia/microphthalmia, anterior segment mesenchymal dysgenesis
Remarks -


Individuals

7 entries on 1 page. Showing entries 1 - 7.
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00090264 - PubMed: Chassaing 2016 Patient P5 - - - - - 0 - - ODA Microphthalmia, cataract, sclerocornea PTCH1 PTCH1 1 1 Michel van Geel
00090967 - PubMed: Chassaing 2016 Family P8 - - - - - 0 - - ODA colobomatous microphthalmia, corpus callosum abnormality and atrial septel defects. PTCH1 PTCH1 1 1 Michel van Geel
00090968 - PubMed: Chassaing 2016 Family P15 - - - - - 0 - - ODA colobomatous microphthalmia, corpus callosum abnormality and atrial septel defects. PTCH1 PTCH1 1 1 Michel van Geel
00091296 - PubMed: Chassaing 2016 Family P17 - - - - - 0 - - ODA bilateral Axenfeld-Rieger malformation PTCH1 PTCH1 1 1 Michel van Geel
00091297 - PubMed: Chassaing 2016 Family P20 - - - - - 0 - - ODA bilateral Peters anomaly PTCH1 PTCH1 1 2 Michel van Geel
00091298 - PubMed: Chassaing 2016 Patient CC-44 - - - - - 0 - - ODA autosomal dominant AM-ASD PTCH1 PTCH1 1 1 Michel van Geel
00091299 - PubMed: Chassaing 2016 Patient CC-10 - - - - - 0 - - ODA bilateral Peters anomaly PTCH1 PTCH1 1 1 Michel van Geel
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