Naegeli–Franceschetti–Jadassohn syndrome

Summary

Naegeli–Franceschetti–Jadassohn syndrome is a developmental defect during embryogenesis^[1]. It draws 15 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #123 of 308).^[2]

Key Facts

• Naegeli–Franceschetti–Jadassohn syndrome's instance of is recorded as developmental defect during embryogenesis^[3].
• Naegeli–Franceschetti–Jadassohn syndrome's instance of is recorded as rare disease^[4].
• Naegeli–Franceschetti–Jadassohn syndrome's instance of is recorded as class of disease^[5].
• Naegeli–Franceschetti–Jadassohn syndrome's subclass of is recorded as ectodermal dysplasia^[6].
• Naegeli–Franceschetti–Jadassohn syndrome's subclass of is recorded as autosomal dominant disease with diffuse palmoplantar keratoderma as a major feature^[7].
• Naegeli–Franceschetti–Jadassohn syndrome's subclass of is recorded as hyperpigmentation of the skin^[8].
• Naegeli–Franceschetti–Jadassohn syndrome's subclass of is recorded as autosomal dominant disease^[9].
• Naegeli–Franceschetti–Jadassohn syndrome's subclass of is recorded as disease^[10].
• Naegeli–Franceschetti–Jadassohn syndrome's MeSH descriptor ID is recorded as C538331^[11].
• Naegeli–Franceschetti–Jadassohn syndrome's OMIM ID is recorded as 161000^[12].
• Naegeli–Franceschetti–Jadassohn syndrome's DiseasesDB is recorded as 29767^[13].
• Naegeli–Franceschetti–Jadassohn syndrome's KEGG ID is recorded as H00708^[14].
• Naegeli–Franceschetti–Jadassohn syndrome's eMedicine ID is recorded as 1117926^[15].
• Naegeli–Franceschetti–Jadassohn syndrome's Disease Ontology ID is recorded as DOID:0111528^[16].
• Naegeli–Franceschetti–Jadassohn syndrome's Orphanet ID is recorded as 69087^[17].
• Naegeli–Franceschetti–Jadassohn syndrome's genetic association is recorded as KRT14^[18].
• Naegeli–Franceschetti–Jadassohn syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_69087^[19].
• Naegeli–Franceschetti–Jadassohn syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111528^[20].
• Naegeli–Franceschetti–Jadassohn syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111528^[21].
• Naegeli–Franceschetti–Jadassohn syndrome's UMLS CUI is recorded as C0343111^[22].
• Naegeli–Franceschetti–Jadassohn syndrome's ICD-10-CM is recorded as Q82.4^[23].
• Naegeli–Franceschetti–Jadassohn syndrome's GARD rare disease ID is recorded as 3912^[24].
• Naegeli–Franceschetti–Jadassohn syndrome's Mondo ID is recorded as MONDO_0008059^[25].
• Naegeli–Franceschetti–Jadassohn syndrome's Microsoft Academic ID is recorded as 2781115779^[26].
• Naegeli–Franceschetti–Jadassohn syndrome's ICD-11 ID is recorded as 352035640^[27].

Why It Matters

Naegeli–Franceschetti–Jadassohn syndrome draws 15 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #123 of 308).^[2] It is known by 7 alternative names across languages and contexts.^[28]