Mowat-Wilson syndrome

Summary

Mowat-Wilson syndrome is a developmental defect during embryogenesis^[1]. It draws 81 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #88 of 308).^[2]

Key Facts

• Mowat-Wilson syndrome's instance of is recorded as developmental defect during embryogenesis^[3].
• Mowat-Wilson syndrome's instance of is recorded as designated intractable/rare disease^[4].
• Mowat-Wilson syndrome's instance of is recorded as rare disease^[5].
• Mowat-Wilson syndrome's instance of is recorded as class of disease^[6].
• Mowat-Wilson syndrome's subclass of is recorded as syndrome^[7].
• Mowat-Wilson syndrome's subclass of is recorded as Hirschsprung's disease^[8].
• Mowat-Wilson syndrome's subclass of is recorded as multiple congenital anomalies/dysmorphic syndrome-intellectual disability^[9].
• Mowat-Wilson syndrome's subclass of is recorded as syndromic intestinal malformation^[10].
• Mowat-Wilson syndrome's subclass of is recorded as genetic syndromic intellectual disability^[11].
• Mowat-Wilson syndrome's subclass of is recorded as genetic disease^[12].
• Mowat-Wilson syndrome's Commons category is recorded as Mowat–Wilson syndrome^[13].
• Mowat-Wilson syndrome's MeSH descriptor ID is recorded as C536990^[14].
• Mowat-Wilson syndrome's OMIM ID is recorded as 235730^[15].
• Mowat-Wilson syndrome's DiseasesDB is recorded as 32975^[16].
• Mowat-Wilson syndrome's Freebase ID is recorded as /m/0f785g^[17].
• Mowat-Wilson syndrome's KEGG ID is recorded as H00908^[18].
• Mowat-Wilson syndrome's GeneReviews ID is recorded as NBK1412^[19].
• Mowat-Wilson syndrome's Disease Ontology ID is recorded as DOID:0060485^[20].
• Mowat-Wilson syndrome's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4594^[21].
• Mowat-Wilson syndrome's Orphanet ID is recorded as 2152^[22].
• Mowat-Wilson syndrome's ICD-9-CM is recorded as 759.89^[23].
• Mowat-Wilson syndrome's NCI Thesaurus ID is recorded as C74999^[24].
• Mowat-Wilson syndrome's genetic association is recorded as ZEB2^[25].
• Mowat-Wilson syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060485^[26].
• Mowat-Wilson syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060485^[27].

Why It Matters

Mowat-Wilson syndrome draws 81 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #88 of 308).^[2] It has Wikipedia articles in 10 language editions, a strong signal of global cultural recognition.^[28] It is known by 13 alternative names across languages and contexts.^[29]