Hereditary cystic kidney disease, known chromosomal abnormality (Q98393): Difference between revisions

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Isso se refere a uma ampla gama de afecções hereditárias, de desenvolvimento e adquiridas. Pode envolver um ou ambos os rins e pode ou não ocorrer na presença de outras anomalias. Este diagnóstico é feito com anomalias cromossômicas conhecidas.
description / endescription / en
 
This refers to a wide range of hereditary, developmental, and acquired conditions. It may involve one or both kidneys and may or may not occur in the presence of other anomalies. This diagnosis is with known chromosomal abnormality.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/1750999140 / rank
 
Normal rank
Property / CURIE
 
CID11:ID_1750999140
Property / CURIE: CID11:ID_1750999140 / rank
 
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Property / Canary Token
 
dki-india-ID_1750999140
Property / Canary Token: dki-india-ID_1750999140 / 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
 
15 August 2026
Timestamp+2026-08-15T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / Collection date: 15 August 2026 / rank
 
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Latest revision as of 14:50, 16 August 2026

This refers to a wide range of hereditary, developmental, and acquired conditions. It may involve one or both kidneys and may or may not occur in the presence of other anomalies. This diagnosis is with known chromosomal abnormality.
Language Label Description Also known as
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ID_1750999140
    English
    Hereditary cystic kidney disease, known chromosomal abnormality
    This refers to a wide range of hereditary, developmental, and acquired conditions. It may involve one or both kidneys and may or may not occur in the presence of other anomalies. This diagnosis is with known chromosomal abnormality.

      Statements

      CID11:ID_1750999140
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      dki-india-ID_1750999140
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      Concluído
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      15 August 2026
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