Fraser syndrome (Q46730): Difference between revisions

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Property / Canonical URI: https://id.who.int/icd/entity/968262849 / rank
 
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CID11:LD2H.0
Property / CURIE: CID11:LD2H.0 / rank
 
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dki-india-LD2H.0
Property / Canary Token: dki-india-LD2H.0 / 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
 
13 August 2026
Timestamp+2026-08-13T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
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Property / Collection date: 13 August 2026 / rank
 
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Property / Linked ICD 10: FLAVIA MARIA DOS SANTOS BERGAMI / rank
 
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Latest revision as of 15:31, 13 August 2026

Fraser syndrome is a rare syndrome characterised by cryptophthalmos and syndactyly and associated with a wide variety of other anomalies including: middle and outer ear malformations; high-arched palate; cleavage along the midplane of nares and tongue; hypertelorism; laryngeal stenosis; wide separation of symphysis pubis; displacement of umbilicus and nipples; absent or multicystic kidneys; bicornuate uterus, malformed Fallopian tubes, fusion of labia and enlargement of clitoris in girls; and undescended testes and small penis with hypospadias in boys.
Language Label Description Also known as
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LD2H.0
    English
    Fraser syndrome
    Fraser syndrome is a rare syndrome characterised by cryptophthalmos and syndactyly and associated with a wide variety of other anomalies including: middle and outer ear malformations; high-arched palate; cleavage along the midplane of nares and tongue; hypertelorism; laryngeal stenosis; wide separation of symphysis pubis; displacement of umbilicus and nipples; absent or multicystic kidneys; bicornuate uterus, malformed Fallopian tubes, fusion of labia and enlargement of clitoris in girls; and undescended testes and small penis with hypospadias in boys.

      Statements

      CID11:LD2H.0
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      dki-india-LD2H.0
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      Concluído
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      13 August 2026
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