Cutis verticis gyrata - retinitis pigmentosa - sensorineural deafness (Q60545): Difference between revisions
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Cutis vertix gyrata - retinite pigmentosa - surdez neurossensorial é uma síndrome hereditária caracterizada por microcefalia, cutis vertix gyrata primária, retinite pigmentosa progressiva, catarata, surdez neurossensorial e déficit intelectual. | |||||||||||||||
| description / en | description / en | ||||||||||||||
Cutis verticis gyrata - retinitis pigmentosa - sensorineural deafness is an inherited syndrome characterised by microcephaly, primary cutis verticis gyrata, progressive retinitis pigmentosa, cataracts, sensorineural deafness and intellectual deficit. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/1711070831 / rank | |||||||||||||||
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CID11:ID_1711070831 | |||||||||||||||
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dki-india-ID_1711070831 | |||||||||||||||
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| 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 08:02, 14 August 2026
Cutis verticis gyrata - retinitis pigmentosa - sensorineural deafness is an inherited syndrome characterised by microcephaly, primary cutis verticis gyrata, progressive retinitis pigmentosa, cataracts, sensorineural deafness and intellectual deficit.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1711070831 |
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| English | Cutis verticis gyrata - retinitis pigmentosa - sensorineural deafness |
Cutis verticis gyrata - retinitis pigmentosa - sensorineural deafness is an inherited syndrome characterised by microcephaly, primary cutis verticis gyrata, progressive retinitis pigmentosa, cataracts, sensorineural deafness and intellectual deficit. |
Statements
CID11:ID_1711070831
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dki-india-ID_1711070831
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Concluído
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13 August 2026
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