A rare inherited form of hypertension characterized by hyperkalemia, hyperchloremic metabolic acidosis, normal or elevated aldosterone, low renin, and normal renal function. [ https://orcid.org/0000-0001-5208-3432 Orphanet:757 ]
Synonyms: chloride shunt syndrome PHAII hyperkalemia-hypertension syndrome, Gordon type Gordon hyperkalemia-hypertension syndrome hypertensive hyperkalemia pseudohypoaldosteronism, type 2 mineralocorticoid resistant hyperkalemia PHA2 pseudohypoaldosteronism, type II familial hyperkalemic hypertension Spitzer-Weinstein syndrome
Term information
- Orphanet:757 (MONDO:equivalentTo)
- SCTID:15689008 (MONDO:equivalentTo)
- GARD:4553 (MONDO:GARD)
- NANDO:2200369 (https://orcid.org/0000-0003-0011-764X)
- ICD9:588.89
- MEDGEN:259599 (MONDO:equivalentTo)
- UMLS:C1449844 (MONDO:equivalentTo)
- icd11.foundation:715347509 (MONDO:equivalentTo)
- OMIMPS:145260 (https://orcid.org/0000-0002-6601-2165)
- NCIT:C123252 (MONDO:equivalentTo)
gard_rare, ordo_disorder, matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, otar, mondo_subtype, matrix_llm__tag_qualy_lost_other, mondo_top_grouping_member, matrix_llm__txgnn_other, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, mondo_top_grouping_urinary_system_disorder, matrix_included, nord_rare, matrix_llm__tag_existing_treatment_other, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, rare, harrisons_view_member, harrisons_view_urinary_system_disorder, harrisons_view_hereditary_disease, orphanet_rare
http://purl.obolibrary.org/obo/NCIT_C123252
http://www.orpha.net/ORDO/Orphanet_757
http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/715347509
http://identifiers.org/medgen/259599
http://linkedlifedata.com/resource/umls/id/C1449844
https://omim.org/phenotypicSeries/PS145260
http://identifiers.org/snomedct/15689008