Aplastic anemia
Symptom Information:
Symptom ID: | HPO:0001915 | ||
Synonyms: |
|
||
Quality: | |||
Cross references: |
|
||
Is a (Direct Parents): |
|
||
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) |