Bone marrow hypocellularity
Symptom Information:
Symptom ID: | HPO:0005528 | ||||||||||
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 bone marrow cell morphology(HPO:0005561) Abnormality of multiple cell lineages in the bone marrow(HPO:0012145) Bone marrow hypocellularity(HPO:0005528) MedDRA: |
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Database Frequency: | 31 / 7739 | ||||||||||
Resource: |
All diseases associated with this symptom:
Albers-Schönberg osteopetrosis | (Orphanet:53) |
Autosomal dominant aplasia and myelodysplasia | (Orphanet:314399) |
BONE MARROW FAILURE SYNDROME 2 | (OMIM:615715) |
Camurati-Engelmann disease | (Orphanet:1328) |
Coats plus syndrome | (Orphanet:313838) |
Cranioectodermal dysplasia 4 | (OMIM:614378) |
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) |
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 2 | (OMIM:613987) |
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 3 | (OMIM:613988) |
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 5 | (OMIM:615190) |
Dyskeratosis congenita | (Orphanet:1775) |
ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNELDEFICIENCY | (OMIM:614520) |
FANCONI ANEMIA, COMPLEMENTATION GROUP F | (OMIM:603467) |
FANCONI ANEMIA, COMPLEMENTATION GROUP I | (OMIM:609053) |
FANCONI ANEMIA, COMPLEMENTATION GROUP J | (OMIM:609054) |
FANCONI ANEMIA, COMPLEMENTATION GROUP L | (OMIM:614083) |
FANCONI ANEMIA, COMPLEMENTATION GROUP Q | (OMIM:615272) |
Ghosal hematodiaphyseal dysplasia | (Orphanet:1802) |
Greenberg dysplasia | (Orphanet:1426) |
Hoyeraal-Hreidarsson syndrome | (Orphanet:3322) |
Idiopathic aplastic anemia | (Orphanet:88) |
Isovaleric acidemia | (Orphanet:33) |
PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 | (OMIM:614742) |
PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 2 | (OMIM:614743) |
Pearson syndrome | (Orphanet:699) |
Primary hypereosinophilic syndrome | (Orphanet:314950) |
Reticular dysgenesis | (Orphanet:33355) |
Retinopathy - anemia- central nervous system anomalies | (Orphanet:3088) |