Muenke syndrome
human disease
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Muenke syndrome
Summary
Muenke syndrome is a developmental defect during embryogenesis[1]. It draws 43 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's subclass of is recorded as craniosynostosis[6].
- Muenke syndrome's subclass of is recorded as syndromic craniosynostosis[7].
- Muenke syndrome's subclass of is recorded as genetic disease[8].
- Muenke syndrome's subclass of is recorded as autosomal dominant disease[9].
- Muenke syndrome's Commons category is recorded as Muenke syndrome[10].
- Muenke syndrome's MeSH descriptor ID is recorded as C537369[11].
- Muenke syndrome's OMIM ID is recorded as 602849[12].
- Muenke syndrome's DiseasesDB is recorded as 33585[13].
- Muenke syndrome's KEGG ID is recorded as H01990[14].
- Muenke syndrome's GeneReviews ID is recorded as NBK1415[15].
- Muenke syndrome's Disease Ontology ID is recorded as DOID:0060703[16].
- Muenke syndrome's Orphanet ID is recorded as 53271[17].
- Muenke syndrome's NCI Thesaurus ID is recorded as C84904[18].
- Muenke syndrome's health specialty is recorded as medical genetics[19].
- Muenke syndrome's genetic association is recorded as FGFR3[20].
- Muenke syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060703[21].
- Muenke syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060703[22].
- Muenke syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_53271[23].
- Muenke syndrome's UMLS CUI is recorded as C1864436[24].
- Muenke syndrome's ICD-10-CM is recorded as Q87.0[25].
- Muenke syndrome's GARD rare disease ID is recorded as 7097[26].
- Muenke syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[27].
Why It Matters
Muenke syndrome draws 43 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.[28] It is known by 8 alternative names across languages and contexts.[29]