Gitelman syndrome
Human disease
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Gitelman syndrome
Summary
Gitelman syndrome is a rare disease[1]. It has Wikipedia articles in 13 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Gitelman syndrome is credited with the discovery of Hillel Jonathan Gitelman[3].
- Gitelman syndrome's instance of is recorded as rare disease[4].
- Gitelman syndrome's instance of is recorded as class of disease[5].
- Hillel Jonathan Gitelman is named after Gitelman syndrome[6].
- Gitelman syndrome is a type of renal tubular transport disease[7].
- Gitelman syndrome is a type of inherited renal tubular disease[8].
- Gitelman syndrome is a type of genetic disease[9].
- Gitelman syndrome is a type of autosomal recessive disease[10].
- Gitelman syndrome is a type of disease[11].
- Gitelman syndrome's Commons category is recorded as Gitelman syndrome[12].
- Gitelman syndrome's ICD-9-CM is recorded as 275.49[13].
- Gitelman syndrome's NCI Thesaurus ID is recorded as C84730[14].
- Gitelman syndrome's health specialty is recorded as nephrology[15].
- Gitelman syndrome's genetic association is recorded as SLC12A3[16].
- Gitelman syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050450[17].
- Gitelman syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0050450[18].
- Gitelman syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_358[19].
- Gitelman syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[20].
Body
Works and Contributions
Gitelman syndrome is credited with the discovery of Hillel Jonathan Gitelman[3].
Why It Matters
Gitelman syndrome has Wikipedia articles in 13 language editions, a strong signal of global cultural recognition.[2] It is known by 10 alternative names across languages and contexts.[21]