Liddle syndrome
genetic disorder inherited in an autosomal dominant manner that is characterized by early, and frequently severe, high blood pressure
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Liddle syndrome
Summary
Liddle syndrome is a rare disease[1]. It has Wikipedia articles in 12 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Liddle syndrome's instance of is recorded as rare disease[3].
- Liddle syndrome's instance of is recorded as class of disease[4].
- Liddle syndrome is a type of renal tubular transport disease[5].
- Liddle syndrome is a type of pseudohyperaldosteronism[6].
- Liddle syndrome is a type of genetic hypertension[7].
- Liddle syndrome is a type of disease[8].
- Liddle syndrome's NCI Thesaurus ID is recorded as C84827[9].
- Liddle syndrome's health specialty is recorded as nephrology[10].
- Liddle syndrome's genetic association is recorded as SCNN1B[11].
- Liddle syndrome's genetic association is recorded as SCNN1G[12].
- Liddle syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050477[13].
- Liddle syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0050477[14].
- Liddle syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_526[15].
- Liddle syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
Why It Matters
Liddle syndrome has Wikipedia articles in 12 language editions, a strong signal of global cultural recognition.[2] It is known by 11 alternative names across languages and contexts.[17]