Muenke syndrome
human disease
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Muenke syndrome
Summary
Muenke syndrome is a developmental defect during embryogenesis[1]. It draws 73 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #115 of 308).[2]
Key Facts
- Muenke syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Muenke syndrome's instance of is recorded as rare disease[4].
- Muenke syndrome's instance of is recorded as class of disease[5].
- Muenke syndrome is a type of craniosynostosis[6].
- Muenke syndrome is a type of syndromic craniosynostosis[7].
- Muenke syndrome is a type of genetic disease[8].
- Muenke syndrome is a type of autosomal dominant disease[9].
- Muenke syndrome's Commons category is recorded as Muenke syndrome[10].
- Muenke syndrome's NCI Thesaurus ID is recorded as C84904[11].
- Muenke syndrome's health specialty is recorded as medical genetics[12].
- Muenke syndrome's genetic association is recorded as FGFR3[13].
- Muenke syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060703[14].
- Muenke syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060703[15].
- Muenke syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_53271[16].
- Muenke syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
Why It Matters
Muenke syndrome draws 73 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #115 of 308).[2] It has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[18] It is known by 8 alternative names across languages and contexts.[19]