hartnup syndrome
1Hartnup syndrome — see under disease …
2Hartnup-Krankheit — Klassifikation nach ICD 10 E72.0 Störungen des Aminosäuretransportes …
3Hartnup-Syndrom — Klassifikation nach ICD 10 E72.0 Störungen des Aminosäuretransportes …
4Hartnup disease — Hart·nup disease härt .nəp n an inherited metabolic disease that is caused by abnormalities of the renal tubules and is characterized esp. by aminoaciduria involving only monocarboxylic monoamines, a dry red scaly rash, and episodic muscular… …
5syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… …
6Hartnup — Surname of British family in which the disease was first described. See H. disease, H. syndrome …
7Fanconi syndrome — Not to be confused with Fanconi anemia. Fanconi syndrome Classification and external resources ICD 10 E72.0 ICD 9 …
8Oculocerebrorenal syndrome — Classification and external resources ICD 10 E72.0 ICD 9 270.8 …
9Hermansky–Pudlak syndrome — Classification and external resources ICD 10 E70.3 (ILDS E70.360) OMIM 203300 …
10Pendred syndrome — Classification and external resources OMIM 274600 DiseasesDB 9771 GeneReviews …
