pseudohypoaldosteronism type 2E
human disease
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pseudohypoaldosteronism type 2E
Summary
pseudohypoaldosteronism type 2E is a rare disease[1].
Key Facts
- pseudohypoaldosteronism type 2E's instance of is recorded as rare disease[2].
- pseudohypoaldosteronism type 2E's instance of is recorded as class of disease[3].
- pseudohypoaldosteronism type 2E's subclass of is recorded as pseudohypoaldosteronism type 2[4].
- pseudohypoaldosteronism type 2E's OMIM ID is recorded as 614496[5].
- pseudohypoaldosteronism type 2E's Orphanet ID is recorded as 300530[6].
- pseudohypoaldosteronism type 2E's genetic association is recorded as CUL3[7].
- pseudohypoaldosteronism type 2E's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_300530[8].
- pseudohypoaldosteronism type 2E's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_757[9].
- pseudohypoaldosteronism type 2E's UMLS CUI is recorded as C3469606[10].
- pseudohypoaldosteronism type 2E's ICD-10-CM is recorded as I15.1[11].
- pseudohypoaldosteronism type 2E's Mondo ID is recorded as MONDO_0013782[12].
- pseudohypoaldosteronism type 2E's UniProt disease ID is recorded as DI-03367[13].