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
iridogoniodysgenesis caused by mutation in FOXC1 C1866560
Anterior segment dysgenesis 3 C1866560
anterior segment dysgenesis 3 C1866560
anterior segment dysgenesis 3, multiple subtypes C1866560
Glaucoma iridogoniodysplasia, familial C1866560
glaucoma iridogoniodysplasia, familial C1866560
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