iridogoniodysgenesis syndrome
Human disease
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Summary
iridogoniodysgenesis syndrome is a developmental defect during embryogenesis[1]. It draws 48 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #135 of 308).[2]
Key Facts
- iridogoniodysgenesis syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- iridogoniodysgenesis syndrome's instance of is recorded as rare disease[4].
- iridogoniodysgenesis syndrome's instance of is recorded as class of disease[5].
- iridogoniodysgenesis syndrome is a type of autosomal dominant disease[6].
- iridogoniodysgenesis syndrome is a type of iris disease[7].
- iridogoniodysgenesis syndrome's genetic association is recorded as PITX2[8].
- iridogoniodysgenesis syndrome's genetic association is recorded as FOXC1[9].
- iridogoniodysgenesis syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050786[10].
- iridogoniodysgenesis syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0050786[11].
- iridogoniodysgenesis syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_91483[12].
- iridogoniodysgenesis syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_98634[13].
- iridogoniodysgenesis syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
Why It Matters
iridogoniodysgenesis syndrome draws 48 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #135 of 308).[2] It is known by 15 alternative names across languages and contexts.[15]