Cutis verticis gyrata - retinitis pigmentosa - sensorineural deafness (Q60545): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
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. | |||
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 |
|---|---|---|---|
| default for all languages | ID_1711070831 |
||
| 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. |
