Ogden syndrome
X-linked disease resulting from a deficiency in N-terminal acetyltransferase, extreme abrupt behavior, anger issues, characterized by postnatal growth failure with severe delays and dysmorphic features in boys
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Ogden syndrome
Summary
Ogden syndrome is a developmental defect during embryogenesis[1]. It draws 626 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #135 of 308).[2]
Key Facts
- Ogden syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Ogden syndrome's instance of is recorded as rare disease[4].
- Ogden syndrome's instance of is recorded as class of disease[5].
- Ogden syndrome is a type of progeroid syndrome[6].
- Ogden syndrome is a type of rare genetic developmental defect during embryogenesis[7].
- Ogden syndrome is a type of X-linked recessive disease[8].
- Ogden syndrome is a type of X-linked dominant disease[9].
- Ogden syndrome is a type of syndrome[10].
- Ogden syndrome is a type of X-linked disease[11].
- Ogden syndrome's NCI Thesaurus ID is recorded as C188215[12].
- Ogden syndrome's genetic association is recorded as NAA10[13].
- Ogden syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050781[14].
- Ogden syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0050781[15].
- Ogden syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_276432[16].
- Ogden syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
Why It Matters
Ogden syndrome draws 626 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #135 of 308).[2] It is known by 10 alternative names across languages and contexts.[18]