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Hartnup disease (also
known as "pellagra-like dermatosis" and "
Hartnup disorder") is an
autosomal recessive metabolic disorder affecting the absorption...
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occur as a
result of alcoholism, long-term diarrhea,
carcinoid syndrome,
Hartnup disease, and a
number of
medications such as isoniazid.
Diagnosis is typically...
- 132. For a full list, see
Hartnup (2004), p. 102
Hartnup (2004), p. 103.
Hartnup (2004), p. 108.
Hartnup (2004), p. 122.
Hartnup (2004), pp. 129–130. Johnston...
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Maple syrup urine disease Homocystinuria Tyrosinemia Trimethylaminuria Hartnup disease Biotinidase deficiency Ornithine carbamoyltransferase deficiency...
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absorbed from the
kidney or intestine.[citation needed] An
example is
Hartnup disease.[citation needed]
Milne MD (1971). "Disorders of
intestinal amino-acid...
- John
Hartnup Jr. (1841 – 21
April 1892) was the
second director of the
Liverpool Observatory (which has
since moved to
become the
Bidston Observatory)...
-
membrane in the
kidney and intestine.
Mutations in the SLC6A19 gene
cause Hartnup disease. GRCh38:
Ensembl release 89: ENSG00000174358 – Ensembl, May 2017...
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denotes 'in the urine').
Elevated levels of
tryptophan are also seen in
Hartnup disease, a
disorder of
amino acid transport. However, the
increase of tryptophan...
- the
transport proteins in the
renal tubule, for example, as
occurs in
Hartnup disease, or may be due to
damage to the
kidney tubule, for example, as...
- are
reabsorbed by
sodium dependent transporters in the
proximal tubule.
Hartnup disease is a
deficiency of the
tryptophan amino acid transporter, which...
