Richards-Rundle syndrome (Q60243): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed label, description and/or aliases in pt-br, en |
Changed an Item |
||
| Property / Canonical URI | |||
| Property / Canonical URI: https://id.who.int/icd/entity/114583632 / rank | |||
Normal rank | |||
Revision as of 07:45, 14 August 2026
Richards-Rundle syndrome is a very rare disorder characterised by autosomal recessive ataxia, hearing loss, mental deterioration, peripheral muscle wasting, hypergonadotrophic hypogonadism and ketoaciduria.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_114583632 |
||
| English | Richards-Rundle syndrome |
Richards-Rundle syndrome is a very rare disorder characterised by autosomal recessive ataxia, hearing loss, mental deterioration, peripheral muscle wasting, hypergonadotrophic hypogonadism and ketoaciduria. |
