Aplastic anemia

Symptom Information:

Symptom ID: HPO:0001915
Synonyms:
Aplastic anemia [OMIM:Aplastic anemia]
Aplastic anemia (in some patients) [OMIM:Aplastic anemia (in some patients)]
Quality:
Cross references:
OMIM: "Aplastic anemia" [OMIM:Aplastic anemia]
OMIM: "Aplastic anemia (in some patients)" [OMIM:Aplastic anemia (in some patients)]
Is a (Direct Parents):
HPO         Pancytopenia
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Abnormality of bone marrow cell morphology(HPO:0005561)
             Abnormality of multiple cell lineages in the bone marrow(HPO:0012145)
                Pancytopenia(HPO:0001876)
                   Aplastic anemia(HPO:0001915)
MedDRA:
Database Frequency: 16 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant aplasia and myelodysplasia (Orphanet:314399)
CHLORAMPHENICOL TOXICITY (OMIM:515000)
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1 (OMIM:127550)
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 2 (OMIM:613989)
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 3 (OMIM:613990)
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 1 (OMIM:224230)
Dubowitz syndrome (Orphanet:235)
Dyskeratosis congenita (Orphanet:1775)
FANCONI ANEMIA, COMPLEMENTATION GROUP N (OMIM:610832)
Idiopathic aplastic anemia (Orphanet:88)
LYMPHOPROLIFERATIVE SYNDROME 2 (OMIM:615122)
Monocytopenia with susceptibility to infections (Orphanet:228423)
PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 (OMIM:614742)
PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 2 (OMIM:614743)
Radio-ulnar synostosis - amegakaryocytic thrombocytopenia (Orphanet:71289)
Retinopathy - anemia- central nervous system anomalies (Orphanet:3088)