Sideroblastic anemia

Symptom Information:

Symptom ID: HPO:0001924
Synonyms:
Hypersideremic anemia [HPO:0001924]
Hypersideremic anemia [Orphanet:48200]
Sideroblastic anemia (disorder) [Orphanet:48160]
Sideroblastic anemia [Orphanet:48160]
Sideroblastic anemia [OMIM:Sideroblastic anemia]
Sideroblastic anaemia [Orphanet:48160]
Sideroblastic anaemia [MedDRA:10040661]
Acquired sideroblastic anaemia [MedDRA:10040661]
Anaemia achrestic [MedDRA:10040661]
Anaemia sideroblastic [MedDRA:10040661]
Anemia achrestic [MedDRA:10040661]
Anemia sideroblastic [MedDRA:10040661]
Sideroblastic anaemia NOS [MedDRA:10040661]
Sideroblastic anemia [MedDRA:10040661]
Acquired sideroblastic anemia [MedDRA:10040661]
Quality:
Cross references:
Orphanet:48200 "Hypersideremic anemia" [Orphanet:48200]
Orphanet:48160 "Sideroblastic anemia" [Orphanet:48160]
OMIM: "Sideroblastic anemia" [OMIM:Sideroblastic anemia]
UMLS:C0002896 "Sideroblastic anemia" [Orphanet:48160]
Is a (Direct Parents):
Orphanet Anemia
HPO         Anemia of inadequate production
MedDRA Anaemias NEC
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)
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)