Haim–Munk syndrome

Summary

Haim–Munk syndrome is a developmental defect during embryogenesis^[1]. It draws 9 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #129 of 308).^[2]

Key Facts

• Haim–Munk syndrome's instance of is recorded as developmental defect during embryogenesis^[3].
• Haim–Munk syndrome's instance of is recorded as rare disease^[4].
• Haim–Munk syndrome's instance of is recorded as class of disease^[5].
• Haim–Munk syndrome's subclass of is recorded as palmoplantar keratosis^[6].
• Haim–Munk syndrome's subclass of is recorded as disorder of lysosomal-related organelles^[7].
• Haim–Munk syndrome's subclass of is recorded as rare genetic developmental defect during embryogenesis^[8].
• Haim–Munk syndrome's subclass of is recorded as autosomal recessive disease with diffuse palmoplantar keratoderma as a major feature^[9].
• Haim–Munk syndrome's subclass of is recorded as malformation syndrome with odontal and/or periodontal component^[10].
• Haim–Munk syndrome's subclass of is recorded as developmental anomaly of metabolic origin^[11].
• Haim–Munk syndrome's MeSH descriptor ID is recorded as C537627^[12].
• Haim–Munk syndrome's OMIM ID is recorded as 245010^[13].
• Haim–Munk syndrome's ICD-10 ID is recorded as Q82.8^[14].
• Haim–Munk syndrome's KEGG ID is recorded as H00696^[15].
• Haim–Munk syndrome's Orphanet ID is recorded as 2342^[16].
• Haim–Munk syndrome's health specialty is recorded as medical genetics^[17].
• Haim–Munk syndrome's genetic association is recorded as CTSC^[18].
• Haim–Munk syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2342^[19].
• Haim–Munk syndrome's UMLS CUI is recorded as C1855627^[20].
• Haim–Munk syndrome's ICD-10-CM is recorded as Q82.8^[21].
• Haim–Munk syndrome's GARD rare disease ID is recorded as 44^[22].
• Haim–Munk syndrome's UK Parliament thesaurus ID is recorded as 443901^[23].
• Haim–Munk syndrome's Mondo ID is recorded as MONDO_0009491^[24].
• Haim–Munk syndrome's Microsoft Academic ID is recorded as 2776707792^[25].
• Haim–Munk syndrome's WikiProjectMed ID is recorded as Haim–Munk syndrome^[26].
• Haim–Munk syndrome's UniProt disease ID is recorded as DI-00539^[27].

Why It Matters

Haim–Munk syndrome draws 9 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #129 of 308).^[2] It has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.^[28] It is known by 8 alternative names across languages and contexts.^[29]