MedGen Find_IDs Find_Terms Annotation
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created at 2024-09-19 07:43:07 UTC
updated at 2024-09-23 18:19:38 UTC
MedGen CUI
Namespace: https://www.ncbi.nlm.nih.gov/medgen/
622,528 entries

There is 0 pattern entry.

Label
Id
vitreoretinochoroidopathy, autosomal dominant C3888099
vitreoretinochoroidopathy, autosomal dominant, with nanophthalmos C3888099
microcornea, Rod-cone dystrophy, cataract, and posterior staphyloma C3888099
Vitreoretinochoroidopathy with microcornea, glaucoma and cataract C3888099
vitreoretinochoroidopathy with microcornea, glaucoma, and cataract C3888099
Autosomal dominant vitreoretinochoroidopathy C3888099
autosomal dominant vitreoretinochoroidopathy C3888099
Autosomal dominant vitreoretinochoroidopathy with nanophthalmos C3888099
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