pseudohypoaldosteronism type 2B
human disease
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pseudohypoaldosteronism type 2B
Summary
pseudohypoaldosteronism type 2B is a rare disease[1].
Key Facts
- pseudohypoaldosteronism type 2B's instance of is recorded as rare disease[2].
- pseudohypoaldosteronism type 2B's instance of is recorded as class of disease[3].
- pseudohypoaldosteronism type 2B's subclass of is recorded as pseudohypoaldosteronism type 2[4].
- pseudohypoaldosteronism type 2B's OMIM ID is recorded as 614491[5].
- pseudohypoaldosteronism type 2B's Orphanet ID is recorded as 88939[6].
- pseudohypoaldosteronism type 2B's genetic association is recorded as WNK4[7].
- pseudohypoaldosteronism type 2B's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_757[8].
- pseudohypoaldosteronism type 2B's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_88939[9].
- pseudohypoaldosteronism type 2B's UMLS CUI is recorded as C1840390[10].
- pseudohypoaldosteronism type 2B's ICD-10-CM is recorded as I15.1[11].
- pseudohypoaldosteronism type 2B's Mondo ID is recorded as MONDO_0013777[12].
- pseudohypoaldosteronism type 2B's UniProt disease ID is recorded as DI-03368[13].