Hypochromic microcytic anemia

Symptom Information:

Symptom ID: HPO:0004840
Synonyms:
Hypochromic, microcytic anemia [HPO:0004840]
Hypochromic, microcytic anemia [OMIM:Hypochromic, microcytic anemia]
Anemia, hypochromic microcytic [OMIM:Anemia, hypochromic microcytic]
Anemia, microcytic hypochromic [OMIM:Anemia, microcytic hypochromic]
Microcytic, hypochromic anemia [OMIM:Microcytic, hypochromic anemia]
Quality:
Cross references:
OMIM: "Hypochromic, microcytic anemia" [OMIM:Hypochromic, microcytic anemia]
OMIM: "Anemia, hypochromic microcytic" [OMIM:Anemia, hypochromic microcytic]
OMIM: "Anemia, microcytic hypochromic" [OMIM:Anemia, microcytic hypochromic]
OMIM: "Microcytic, hypochromic anemia" [OMIM:Microcytic, hypochromic anemia]
Is a (Direct Parents):
HPO         Hypochromic anemia
HPO         Microcytic anemia
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Abnormality of erythrocytes(HPO:0001877)
             Anemia(HPO:0001903)
                Anemia of inadequate production(HPO:0010972)
                   Hypochromic anemia(HPO:0001931)
                      Hypochromic microcytic anemia(HPO:0004840)
                   Microcytic anemia(HPO:0001935)
                      Hypochromic microcytic anemia(HPO:0004840)
MedDRA:
Database Frequency: 15 / 7739
Resource:

All diseases associated with this symptom:

Alpha-thalassemia (Orphanet:846)
Alpha-thalassemia - X-linked intellectual deficit syndrome (Orphanet:847)
Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16 (Orphanet:98791)
Alpha-thalassemia - myelodysplastic syndrome (Orphanet:231401)
Beta-thalassemia major (Orphanet:231214)
Craniofacial dysplasia-osteopenia syndrome (Orphanet:314555)
HEMOGLOBIN--ALPHA LOCUS 1 (OMIM:141800)
IRIDA syndrome (Orphanet:209981)
Isolated sedoheptulokinase deficiency (ORPHA:440713)
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia (Orphanet:363972)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency (Orphanet:88618)
SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS,AND DEVELOPMENTAL DELAY (OMIM:616084)
X-linked sideroblastic anemia (Orphanet:75563)
X-linked sideroblastic anemia - ataxia (Orphanet:2802)