Fanconi syndrome
renal tubular transport disease of the proximal renal tubes characterized by glucosuria, phosphaturia, generalized aminoaciduria and HCO3 wasting
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Fanconi syndrome
Summary
Fanconi syndrome is a rare disease[1]. It has Wikipedia articles in 18 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Fanconi syndrome's instance of is recorded as rare disease[3].
- Fanconi syndrome's instance of is recorded as class of disease[4].
- Guido Fanconi is named after Fanconi syndrome[5].
- Fanconi syndrome is a type of renal tubular transport disease[6].
- Fanconi syndrome is a type of disease[7].
- Fanconi syndrome's ICPC 2 ID is recorded as T99[8].
- Fanconi syndrome's NCI Thesaurus ID is recorded as C3034[9].
- Fanconi syndrome's NCI Thesaurus ID is recorded as C4377[10].
- Fanconi syndrome's different from is recorded as Fanconi anemia[11].
- Fanconi syndrome's health specialty is recorded as nephrology[12].
- Fanconi syndrome's health specialty is recorded as endocrinology[13].
- Fanconi syndrome's genetic association is recorded as SLC34A1[14].
- Fanconi syndrome's genetic association is recorded as EHHADH[15].
- Fanconi syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_1062[16].
- Fanconi syndrome's exact match is recorded as http://identifiers.org/doid/DOID:1062[17].
- Fanconi syndrome's exact match is recorded as http://purl.obolibrary.org/obo/HP_0001994[18].
- Fanconi syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_3337[19].
- Fanconi syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[20].
Why It Matters
Fanconi syndrome has Wikipedia articles in 18 language editions, a strong signal of global cultural recognition.[2] It is known by 30 alternative names across languages and contexts.[21]