Iron deficiency anemia
Symptom Information:
Symptom ID: | HPO:0001891 | ||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |