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
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Abderhalden–Kaufmann–Lignac syndrome
Summary
Abderhalden–Kaufmann–Lignac syndrome is a disease[1]. It draws 10 Wikipedia views per month (disease category, ranking #279 of 806).[2]
Key Facts
- Abderhalden–Kaufmann–Lignac syndrome's instance of is recorded as disease[3].
- Abderhalden–Kaufmann–Lignac syndrome is a type of cystinosis[4].
- Abderhalden–Kaufmann–Lignac syndrome is a type of cystinosis, nephropathic[5].
- Abderhalden–Kaufmann–Lignac syndrome's Commons category is recorded as Abderhalden–Kaufmann–Lignac syndrome[6].
- Abderhalden–Kaufmann–Lignac syndrome's NCI Thesaurus ID is recorded as C129932[7].
Why It Matters
Abderhalden–Kaufmann–Lignac syndrome draws 10 Wikipedia views per month (disease category, ranking #279 of 806).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[8] It is known by 7 alternative names across languages and contexts.[9]