Abderhalden–Kaufmann–Lignac syndrome (Q4664900)

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rare autosomal-recessive, lysomal storage childhood disorder involving deposits of cystine crystals in various parts of the body, including the bone marrow, conjunctiva and cornea
  • Abderhalden-Kaufmann-Lignac syndrome
  • nephropathic cystinosis
  • Abderhalden Kaufmann Lignac syndrome
  • Abderhalden Lignac Kaufmann disease
  • Abderhalden-Lignac-Kaufmann disease
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Language Label Description Also known as
English
Abderhalden–Kaufmann–Lignac syndrome
rare autosomal-recessive, lysomal storage childhood disorder involving deposits of cystine crystals in various parts of the body, including the bone marrow, conjunctiva and cornea
  • Abderhalden-Kaufmann-Lignac syndrome
  • nephropathic cystinosis
  • Abderhalden Kaufmann Lignac syndrome
  • Abderhalden Lignac Kaufmann disease
  • Abderhalden-Lignac-Kaufmann disease

Statements

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C129932
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Abderhalden–Kaufmann–Lignac syndrome
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Identifiers

 
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