Schindler disease
Rare congenital metabolic disorder in humans.
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Schindler disease
Summary
Schindler disease is a congenital disorder[1]. It has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Schindler disease's instance of is recorded as congenital disorder[3].
- Schindler disease's instance of is recorded as rare disease[4].
- Schindler disease's instance of is recorded as class of disease[5].
- Detlev Schindler is named after Schindler disease[6].
- Schindler disease is a type of lysosomal storage disease[7].
- Schindler disease is a type of autosomal recessive disease[8].
- Schindler disease's ICD-9-CM is recorded as 277.89[9].
- Schindler disease's health specialty is recorded as endocrinology[10].
- Schindler disease's genetic association is recorded as NAGA[11].
- Schindler disease's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0112317[12].
- Schindler disease's exact match is recorded as http://identifiers.org/doid/DOID:0112317[13].
Why It Matters
Schindler disease has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2] It is known by 10 alternative names across languages and contexts.[14]