Bone marrow hypocellularity

Symptom Information:

Symptom ID: HPO:0005528
Synonyms:
Bone marrow failure [HPO:0005528]
Bone marrow hypoplasia [HPO:0005528]
Hypoplastic bone marrow [HPO:0005528]
Bone marrow failure [OMIM:Bone marrow failure]
Bone marrow hypoplasia [OMIM:Bone marrow hypoplasia]
Hypoplastic bone marrow [OMIM:Hypoplastic bone marrow]
Bone marrow failure (1 patient) [OMIM:Bone marrow failure (1 patient)]
Bone marrow failure (classic feature, NOLA3 patient) [OMIM:Bone marrow failure (classic feature, NOLA3 patient)]
Bone marrow failure (in some patients) [OMIM:Bone marrow failure (in some patients)]
Bone marrow hypoplasia (in some patients) [OMIM:Bone marrow hypoplasia (in some patients)]
Quality:
Cross references:
OMIM: "Bone marrow failure" [OMIM:Bone marrow failure]
OMIM: "Bone marrow hypoplasia" [OMIM:Bone marrow hypoplasia]
OMIM: "Hypoplastic bone marrow" [OMIM:Hypoplastic bone marrow]
OMIM: "Bone marrow failure (1 patient)" [OMIM:Bone marrow failure (1 patient)]
OMIM: "Bone marrow failure (classic feature, NOLA3 patient)" [OMIM:Bone marrow failure (classic feature, NOLA3 patient)]
OMIM: "Bone marrow failure (in some patients)" [OMIM:Bone marrow failure (in some patients)]
OMIM: "Bone marrow hypoplasia (in some patients)" [OMIM:Bone marrow hypoplasia (in some patients)]
Is a (Direct Parents):
HPO         Abnormality of multiple cell lineages in the bone marrow
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:
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)