hereditary haemolytic anaemia due to red cell membrane defects (Q55789123)

From Wikidata
Revision as of 19:43, 26 February 2024 by KrBot (talk | contribs) (‎Changed reference of claim: subclass of (P279): congenital hemolytic anemia (Q5160435), см. / see autofix на / on Property talk:P5270)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Jump to navigation Jump to search
human disease
  • constitutional hemolytic anemia due to a red cell membrane anomaly
edit
Language Label Description Also known as
English
hereditary haemolytic anaemia due to red cell membrane defects
human disease
  • constitutional hemolytic anemia due to a red cell membrane anomaly

Statements

NCI Thesaurus ID
C101218
0 references

Identifiers

Mondo ID
MONDO_0020101
0 references
 
edit
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit
                    Retrieved from "https://www.wikidata.org/w/index.php?title=Q55789123&oldid=2088077012"