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 9 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's subclass of is recorded as cystinosis[4].
- Abderhalden–Kaufmann–Lignac syndrome's subclass of is recorded as cystinosis, nephropathic[5].
- Abderhalden–Kaufmann–Lignac syndrome's Commons category is recorded as Abderhalden–Kaufmann–Lignac syndrome[6].
- Abderhalden–Kaufmann–Lignac syndrome's MeSH descriptor ID is recorded as C535335[7].
- Abderhalden–Kaufmann–Lignac syndrome's OMIM ID is recorded as 219800[8].
- Abderhalden–Kaufmann–Lignac syndrome's ICD-9 ID is recorded as 270.0[9].
- Abderhalden–Kaufmann–Lignac syndrome's Encyclopædia Britannica Online ID is recorded as topic/nephropathic-cystinosis[10].
- Abderhalden–Kaufmann–Lignac syndrome's NCI Thesaurus ID is recorded as C129932[11].
- Abderhalden–Kaufmann–Lignac syndrome's UMLS CUI is recorded as C2930877[12].
- Abderhalden–Kaufmann–Lignac syndrome's GARD rare disease ID is recorded as 10074[13].
- Abderhalden–Kaufmann–Lignac syndrome's Mondo ID is recorded as MONDO_0021725[14].
- Abderhalden–Kaufmann–Lignac syndrome's WikiProjectMed ID is recorded as Abderhalden–Kaufmann–Lignac syndrome[15].
Why It Matters
Abderhalden–Kaufmann–Lignac syndrome draws 9 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.[16] It is known by 7 alternative names across languages and contexts.[17]