Atypical hypotonia-cystinuria syndrome (Q66532): Difference between revisions

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+https://id.who.int/icd/entity/1982772708
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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.