MEHMO syndrome (Q87530): Difference between revisions

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description / pt-brdescription / pt-br
 
A síndrome MEHMO é caracterizada por déficit intelectual grave, epilepsia, microcefalia, hipogenitalismo e obesidade. Atraso no crescimento e diabetes também estão presentes.
description / endescription / en
 
MEHMO syndrome is characterised by severe intellectual deficit, epilepsy, microcephaly, hypogenitalism and obesity. Growth delay and diabetes are also present.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/500681653 / rank
 
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Property / CURIE
 
CID11:ID_500681653
Property / CURIE: CID11:ID_500681653 / rank
 
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Property / Canary Token
 
dki-india-ID_500681653
Property / Canary Token: dki-india-ID_500681653 / rank
 
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Property / Verification Status
 
Concluído
Property / Verification Status: Concluído / rank
 
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Property / Knowledge Architect
 
Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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Property / Collection date
 
13 August 2026
Timestamp+2026-08-13T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
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After0
Property / Collection date: 13 August 2026 / rank
 
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Latest revision as of 13:11, 15 August 2026

MEHMO syndrome is characterised by severe intellectual deficit, epilepsy, microcephaly, hypogenitalism and obesity. Growth delay and diabetes are also present.
Language Label Description Also known as
default for all languages
ID_500681653
    English
    MEHMO syndrome
    MEHMO syndrome is characterised by severe intellectual deficit, epilepsy, microcephaly, hypogenitalism and obesity. Growth delay and diabetes are also present.

      Statements

      CID11:ID_500681653
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      dki-india-ID_500681653
      0 references
      Concluído
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      13 August 2026
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