FG syndrome (Q94172): Difference between revisions

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Property / Canonical URI: https://id.who.int/icd/entity/156523187 / rank
 
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CID11:ID_156523187
Property / CURIE: CID11:ID_156523187 / rank
 
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dki-india-ID_156523187
Property / Canary Token: dki-india-ID_156523187 / rank
 
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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
 
15 August 2026
Timestamp+2026-08-15T00:00:00Z
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CalendarGregorian
Precision1 day
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Property / Collection date: 15 August 2026 / rank
 
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Latest revision as of 09:17, 16 August 2026

FG syndrome (FGS) is a X-linked recessive multiple congenital anomalies (MCA) and developmental delay syndrome with a characteristic psychological pattern (delayed development of sensory integration, attention deficit disorder, self-absorption and fascinations with mechanical toys and objects). Males are affected, but carrier girls and women may also be affected, sometimes more severely than the males.
Language Label Description Also known as
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ID_156523187
    English
    FG syndrome
    FG syndrome (FGS) is a X-linked recessive multiple congenital anomalies (MCA) and developmental delay syndrome with a characteristic psychological pattern (delayed development of sensory integration, attention deficit disorder, self-absorption and fascinations with mechanical toys and objects). Males are affected, but carrier girls and women may also be affected, sometimes more severely than the males.

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      CID11:ID_156523187
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      dki-india-ID_156523187
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      Concluído
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      15 August 2026
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