Amenorrhoea due to disorders of the ovary (Q53118): Difference between revisions
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Disgenesia gonadal, Síndrome de Turner, Síndrome de Swyer (disgenesia gonadal 46XY), disgenesia gonadal 46XX, falência ovariana prematura (causada por anormalidades cromossômicas, permutações X frágil, transtornos autoimunes, radioterapia, quimioterapia, galactosemia ou distúrbios genéticos raros de depleção folicular acelerada) | |||||||||||||||
| description / en | description / en | ||||||||||||||
Gonadal dysgenesis, Turner Syndrome, Swyer Syndrome (46XY gonadal dysgenesis), 46XX gonadal dysgenesis, premature ovarian failure (caused by chromosomal abnormalities, Fragile X permutations, autoimmune disorders, radiation therapy, chemotherapy, galactosemia or rare genetic disorders of accelerated follicular depletion) | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/1282106936 / rank | |||||||||||||||
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CID11:ID_1282106936 | |||||||||||||||
| Property / CURIE: CID11:ID_1282106936 / rank | |||||||||||||||
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dki-india-ID_1282106936 | |||||||||||||||
| Property / Canary Token: dki-india-ID_1282106936 / rank | |||||||||||||||
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Concluído | |||||||||||||||
| Property / Verification Status: Concluído / rank | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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13 August 2026
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| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
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Latest revision as of 00:32, 14 August 2026
Gonadal dysgenesis, Turner Syndrome, Swyer Syndrome (46XY gonadal dysgenesis), 46XX gonadal dysgenesis, premature ovarian failure (caused by chromosomal abnormalities, Fragile X permutations, autoimmune disorders, radiation therapy, chemotherapy, galactosemia or rare genetic disorders of accelerated follicular depletion)
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1282106936 |
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| English | Amenorrhoea due to disorders of the ovary |
Gonadal dysgenesis, Turner Syndrome, Swyer Syndrome (46XY gonadal dysgenesis), 46XX gonadal dysgenesis, premature ovarian failure (caused by chromosomal abnormalities, Fragile X permutations, autoimmune disorders, radiation therapy, chemotherapy, galactosemia or rare genetic disorders of accelerated follicular depletion) |
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CID11:ID_1282106936
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dki-india-ID_1282106936
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Concluído
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13 August 2026
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