Sideroblastic anemia
Symptom Information:
Symptom ID: | HPO:0001924 | |||||||||||||||
Synonyms: |
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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) Sideroblastic anemia(HPO:0001924) MedDRA: Blood and lymphatic system disorders(MedDRA:10005329) Anaemias nonhaemolytic and marrow depression(MedDRA:10002086) Anaemias NEC(MedDRA:10002067) Sideroblastic anemia(HPO:0001924) |
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Database Frequency: | 12 / 7739 | |||||||||||||||
Resource: |
All diseases associated with this symptom:
ANEMIA, SIDEROBLASTIC, AUTOSOMAL DOMINANT | (OMIM:182170) |
Hereditary myopathy with lactic acidosis due to ISCU deficiency | (Orphanet:43115) |
Kearns-Sayre syndrome | (Orphanet:480) |
Myopathy, lactic acidosis, and sideroblastic anemia 1; MLASA1 | (OMIM:600462) |
Myopathy, lactic acidosis, and sideroblastic anemia 2; MLASA2 | (OMIM:613561) |
Pearson syndrome | (Orphanet:699) |
SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS,AND DEVELOPMENTAL DELAY | (OMIM:616084) |
Thiamine-responsive megaloblastic anemia syndrome | (Orphanet:49827) |
Wolfram syndrome 1 | (OMIM:222300) |
Wolfram syndrome, mitochondrial form | (OMIM:598500) |
X-linked sideroblastic anemia | (Orphanet:75563) |
X-linked sideroblastic anemia - ataxia | (Orphanet:2802) |