Iron deficiency anemia

Symptom Information:

Symptom ID: HPO:0001891
Synonyms:
Iron-deficiency anemia [HPO:0001891]
Iron deficiency (disorder) [Orphanet:48220]
Iron deficiency anemia (disorder) [Orphanet:48220]
Iron deficiency anemia [Orphanet:48220]
Iron deficiency [Orphanet:48220]
Iron deficiency anemia [OMIM:Iron deficiency anemia]
Iron-deficiency anemia [OMIM:Iron-deficiency anemia]
Ferropenic anemia [Orphanet:48220]
Iron deficiency anaemia [Orphanet:48220]
Iron deficiency [MedDRA:10022970]
Hypoferrism [MedDRA:10022970]
Iron deficiency anaemia [MedDRA:10022972]
Anaemia iron deficiency [MedDRA:10022972]
Anemia iron deficiency [MedDRA:10022972]
Iron def anaemia [MedDRA:10022972]
Iron deficiency anaemias [MedDRA:10022972]
Iron deficiency anemia [MedDRA:10022972]
Iron deficiency anemia secondary to blood loss (chronic) [MedDRA:10022972]
Iron deficiency anemia secondary to inadequate dietary iron intake [MedDRA:10022972]
Iron deficiency anemia, unspecified [MedDRA:10022972]
Iron deficiency anemias [MedDRA:10022972]
Other specified iron deficiency anemias [MedDRA:10022972]
Sideropenic anaemia [MedDRA:10022972]
Sideropenic anemia [MedDRA:10022972]
Iron deficiency anaemia secondary to blood loss (chronic) [MedDRA:10022972]
Iron deficiency anaemia secondary to inadequate dietary iron intake [MedDRA:10022972]
Iron deficiency anaemia, unspecified [MedDRA:10022972]
Asiderotic anaemia [MedDRA:10022972]
Asiderotic anemia [MedDRA:10022972]
Chronic iron deficiency anemia [MedDRA:10022972]
Chronic iron deficiency anaemia [MedDRA:10022972]
Ferropenic anemia [MedDRA:10022972]
Ferropenic anaemia [MedDRA:10022972]
Anaemia from chronic blood loss [MedDRA:10022972]
Anemia from chronic blood loss [MedDRA:10022972]
Iron deficiency [OMIM:Iron deficiency]
Iron deficiency (in some patients) [OMIM:Iron deficiency (in some patients)]
Iron deficiency anemia (adults) [OMIM:Iron deficiency anemia (adults)]
Iron-deficiency anemia (in some patients) [OMIM:Iron-deficiency anemia (in some patients)]
Iron deficiencies [MedDRA:10022971]
Quality:
Cross references:
Orphanet:48220 "Ferropenic anemia" [Orphanet:48220]
OMIM: "Iron deficiency anemia" [OMIM:Iron deficiency anemia]
OMIM: "Iron-deficiency anemia" [OMIM:Iron-deficiency anemia]
OMIM: "Iron deficiency" [OMIM:Iron deficiency]
OMIM: "Iron deficiency (in some patients)" [OMIM:Iron deficiency (in some patients)]
OMIM: "Iron deficiency anemia (adults)" [OMIM:Iron deficiency anemia (adults)]
OMIM: "Iron-deficiency anemia (in some patients)" [OMIM:Iron-deficiency anemia (in some patients)]
UMLS:C0162316 "Iron deficiency anemia" [Orphanet:48220]
UMLS:C0240066 "Iron deficiency" [Orphanet:48220]
Is a (Direct Parents):
Orphanet Anemia
HPO         Hypochromic anemia
MedDRA Iron and trace metal metabolism disorders
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)
                      Iron deficiency anemia(HPO:0001891)
MedDRA:
Metabolism and nutrition disorders(MedDRA:10027433)
    Iron and trace metal metabolism disorders(MedDRA:10022958)
       Iron deficiency anemia(HPO:0001891)
Database Frequency: 22 / 7739
Resource:

All diseases associated with this symptom:

AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME (OMIM:601859)
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA (OMIM:603909)
Autoimmune lymphoproliferative syndrome (Orphanet:3261)
Autoimmune polyendocrinopathy type 2 (Orphanet:3143)
BILE ACID SYNTHESIS DEFECT, CONGENITAL, 5 (OMIM:616278)
BREATH-HOLDING SPELLS (OMIM:607578)
Blue rubber bleb nevus (Orphanet:1059)
CANDIDIASIS, FAMILIAL, 2 (OMIM:212050)
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 (OMIM:212750)
ENTEROPATHY, PROTEIN-LOSING (OMIM:226300)
GOLGI REASSEMBLY STACKING PROTEIN 1 (OMIM:606867)
IRIDA syndrome (Orphanet:209981)
Idiopathic pulmonary hemosiderosis (Orphanet:99931)
Jervell and Lange-Nielsen syndrome (Orphanet:90647)
Menetrier disease (Orphanet:2494)
PHOSPHOLIPASE A2, GROUP IVA (OMIM:600522)
PROTOPORPHYRIA, ERYTHROPOIETIC, X-LINKED (OMIM:300752)
PULMONARY HEMOSIDEROSIS (OMIM:178550)
Peutz-Jeghers syndrome (Orphanet:2869)
Primary intestinal lymphangiectasia (Orphanet:90362)
WISKOTT-ALDRICH SYNDROME (OMIM:301000)
WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM (OMIM:600903)