Abnormality of blood and blood-forming tissues

Symptom Information:

Symptom ID: HPO:0001871
Synonyms:
Abnormality of the haematopoietic system [HPO:0001871]
Abnormality of the hematopoietic system [HPO:0001871]
Hematologic disease [HPO:0001871]
Hematological abnormality [HPO:0001871]
Hematological anomaly [Orphanet:48000]
Anomalies of the hematological system [Orphanet:48000]
Quality:
Cross references:
Orphanet:48000 "Anomalies of the hematological system" [Orphanet:48000]
Is a (Direct Parents):
HPO         Phenotypic abnormality
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
MedDRA:
Database Frequency: 37 / 7739
Resource:

All diseases associated with this symptom:

Angio-osteohypertrophic syndrome (Orphanet:2346)
Bietti crystalline dystrophy (Orphanet:41751)
CANDIDIASIS, FAMILIAL, 2 (OMIM:212050)
COUMARIN RESISTANCE (OMIM:122700)
Chylomicron retention disease (Orphanet:71)
Cryoglobulinemic vasculitis (Orphanet:91138)
Dorfman-Chanarin disease (Orphanet:98907)
EOSINOPHILOPENIA (OMIM:131430)
FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 2 (OMIM:142470)
FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 3 (OMIM:305435)
FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 5 (OMIM:142335)
FLOOD FACTOR DEFICIENCY (OMIM:136150)
FUCOSYLTRANSFERASE 1 (OMIM:211100)
Fanconi anemia (Orphanet:84)
GIANT NEUTROPHIL LEUKOCYTES (OMIM:137500)
GM1 gangliosidosis type 3 (Orphanet:79257)
GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR RECEPTOR, ALPHA SUBUNIT,Y-CHROMOSOMAL (OMIM:425000)
HEMOGLOBIN, HIGH ALTITUDE ADAPTATION (OMIM:609070)
HEMOPOIETIC PROLIFERATION (OMIM:306930)
INTERLEUKIN 3 RECEPTOR, Y-CHROMOSOMAL (OMIM:430000)
Ichthyosis - hypotrichosis - sclerosing cholangitis (Orphanet:59303)
LEUKOCYTE NUCLEAR APPENDAGES, HEREDITARY PREVALENCE OF (OMIM:151500)
MACROCYTOSIS, FAMILIAL (OMIM:600084)
Mendelian susceptibility to mycobacterial diseases (Orphanet:748)
Myeloperoxidase deficiency (Orphanet:2587)
PELGER-HUET-LIKE ANOMALY AND EPISODIC FEVER WITH ABDOMINAL PAIN (OMIM:260570)
PHAGOCYTOSIS, PLASMA-RELATED DEFECT IN (OMIM:171100)
PREMATURE AGING SYNDROME, OKAMOTO TYPE (OMIM:601811)
Primary cutaneous lymphoma (Orphanet:542)
RHEUMATOID ARTHRITIS (OMIM:180300)
SULFHEMOGLOBINEMIA, CONGENITAL (OMIM:185460)
Severe combined immunodeficiency due to adenosine deaminase deficiency (Orphanet:277)
Systemic mastocytosis (Orphanet:2467)
Thiopurine S-methyltransferase deficiency (Orphanet:3315)
X-linked intellectual deficit - hypotonic face (Orphanet:73220)
XG REGULATOR (OMIM:489500)
Yunis-Varon syndrome (Orphanet:3472)