pseudohypoaldosteronism type 2D
human disease
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pseudohypoaldosteronism type 2D
Summary
pseudohypoaldosteronism type 2D is a rare disease[1].
Key Facts
- pseudohypoaldosteronism type 2D's instance of is recorded as rare disease[2].
- pseudohypoaldosteronism type 2D's instance of is recorded as class of disease[3].
- pseudohypoaldosteronism type 2D's subclass of is recorded as pseudohypoaldosteronism type 2[4].
- pseudohypoaldosteronism type 2D's OMIM ID is recorded as 614495[5].
- pseudohypoaldosteronism type 2D's Orphanet ID is recorded as 300525[6].
- pseudohypoaldosteronism type 2D's genetic association is recorded as KLHL3[7].
- pseudohypoaldosteronism type 2D's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_300525[8].
- pseudohypoaldosteronism type 2D's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_757[9].
- pseudohypoaldosteronism type 2D's UMLS CUI is recorded as C3469605[10].
- pseudohypoaldosteronism type 2D's ICD-10-CM is recorded as I15.1[11].
- pseudohypoaldosteronism type 2D's Mondo ID is recorded as MONDO_0013781[12].
- pseudohypoaldosteronism type 2D's UniProt disease ID is recorded as DI-03366[13].