Atypical hypotonia-cystinuria syndrome (Q66532): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| Property / Collection date | |||||||||||||||
13 August 2026
| |||||||||||||||
| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest revision as of 14:21, 14 August 2026
A condition characterised by neonatal and infantile hypotonia, poor feeding in neonates, growth retardation due to growth hormone deficiency, mild facial dysmorphism and cystinuria type I.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1982772708 |
||
| English | Atypical hypotonia-cystinuria syndrome |
A condition characterised by neonatal and infantile hypotonia, poor feeding in neonates, growth retardation due to growth hormone deficiency, mild facial dysmorphism and cystinuria type I. |
Statements
CID11:ID_1982772708
0 references
dki-india-ID_1982772708
0 references
Concluído
0 references
13 August 2026
0 references
