Pancytopenia
Symptom Information:
Symptom ID: | HPO:0001876 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||
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) Pancytopenia(HPO:0001876) MedDRA: Blood and lymphatic system disorders(MedDRA:10005329) Anaemias nonhaemolytic and marrow depression(MedDRA:10002086) Marrow depression and hypoplastic anaemias(MedDRA:10026847) Pancytopenia(HPO:0001876) |
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Database Frequency: | 89 / 7739 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
AICARDI-GOUTIERES SYNDROME 4 | (OMIM:610333) |
AUTOINFLAMMATION WITH INFANTILE ENTEROCOLITIS | (OMIM:616050) |
Adult Still's disease | (Orphanet:829) |
Aggressive systemic mastocytosis | (Orphanet:98850) |
Albers-Schönberg osteopetrosis | (Orphanet:53) |
Ataxia - pancytopenia | (Orphanet:2585) |
Autosomal dominant aplasia and myelodysplasia | (Orphanet:314399) |
Autosomal recessive lymphoproliferative disease | (Orphanet:238505) |
Autosomal recessive malignant osteopetrosis | (Orphanet:667) |
Bangstad syndrome | (Orphanet:1227) |
Beta-thalassemia major | (Orphanet:231214) |
COENZYME Q10 DEFICIENCY, PRIMARY, 1 | (OMIM:607426) |
Coats plus syndrome | (Orphanet:313838) |
Congenital amegakaryocytic thrombocytopenia | (Orphanet:3319) |
Constitutional megaloblastic anemia with severe neurologic disease | (Orphanet:319651) |
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) |
Deafness - intellectual deficit, Martin-Probst type | (Orphanet:85321) |
Deafness - lymphedema - leukemia | (Orphanet:3226) |
Dyskeratosis congenita | (Orphanet:1775) |
ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNELDEFICIENCY | (OMIM:614520) |
FANCONI ANEMIA, COMPLEMENTATION GROUP A | (OMIM:227650) |
FANCONI ANEMIA, COMPLEMENTATION GROUP C | (OMIM:227645) |
FANCONI ANEMIA, COMPLEMENTATION GROUP D2 | (OMIM:227646) |
FANCONI ANEMIA, COMPLEMENTATION GROUP E | (OMIM:600901) |
FANCONI ANEMIA, COMPLEMENTATION GROUP P | (OMIM:613951) |
FANCONI-LIKE SYNDROME | (OMIM:227850) |
Fanconi anemia | (Orphanet:84) |
Felty syndrome | (Orphanet:47612) |
Gaucher disease | (Orphanet:355) |
Gaucher disease - ophthalmoplegia - cardiovascular calcification | (Orphanet:2072) |
Gaucher disease type 1 | (Orphanet:77259) |
Gaucher disease type 2 | (Orphanet:77260) |
Gaucher disease type 3 | (Orphanet:77261) |
Ghosal hematodiaphyseal dysplasia | (Orphanet:1802) |
Griscelli disease | (Orphanet:381) |
Griscelli disease type 2 | (Orphanet:79477) |
Hairy cell leukemia variant | (Orphanet:300878) |
Hashimoto-Pritzker syndrome | (Orphanet:99872) |
Hereditary folate malabsorption | (Orphanet:90045) |
Hodgkin lymphoma | (Orphanet:98293) |
Hodgkin lymphoma, classical | (Orphanet:391) |
Hoyeraal-Hreidarsson syndrome | (Orphanet:3322) |
Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome | (Orphanet:363694) |
IMMUNODEFICIENCY 16 | (OMIM:615593) |
IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY | (OMIM:614700) |
INTRAUTERINE GROWTH RETARDATION WITH INCREASED MITOMYCIN C SENSITIVITY | (OMIM:600546) |
Isovaleric acidemia | (Orphanet:33) |
Jacobsen syndrome | (Orphanet:2308) |
LIG4 syndrome | (Orphanet:99812) |
LYMPHOID SYSTEM DETERIORATION, PROGRESSIVE | (OMIM:247630) |
LYMPHOPROLIFERATIVE SYNDROME 1 | (OMIM:613011) |
LYMPHOPROLIFERATIVE SYNDROME 2 | (OMIM:615122) |
LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1 | (OMIM:308240) |
Legionellosis | (Orphanet:549) |
Methylmalonic acidemia with homocystinuria | (Orphanet:26) |
Methylmalonic acidemia with homocystinuria, type cblF | (Orphanet:79284) |
Nodular lymphocyte predominant Hodgkin lymphoma | (Orphanet:86893) |
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1 | (OMIM:259700) |
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2 | (OMIM:259710) |
Osteopetrosis | (Orphanet:2781) |
PANCYTOPENIA AND OCCLUSIVE VASCULAR DISEASE | (OMIM:167850) |
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) |
Propionic acidemia | (Orphanet:35) |
Pyogenic arthritis - pyoderma gangrenosum - acne | (Orphanet:69126) |
RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER | (OMIM:614470) |
Radio-ulnar synostosis - amegakaryocytic thrombocytopenia | (Orphanet:71289) |
SECKEL SYNDROME 1 | (OMIM:210600) |
SPLENOMEGALY SYNDROME WITH SPLENIC GERMINAL CENTER HYPOPLASIA ANDREDUCED CIRCULATING T HELPER CELLS | (OMIM:183350) |
SPLENOMEGALY, CYTOPENIA, AND VISION LOSS | (OMIM:614979) |
Sarcoidosis | (Orphanet:797) |
Seckel syndrome | (Orphanet:808) |
Shwachman-Diamond syndrome | (Orphanet:811) |
Systemic mastocytosis | (Orphanet:2467) |
Thymoma | (Orphanet:99867) |
Transaldolase deficiency | (Orphanet:101028) |
Transcobalamin deficiency | (Orphanet:859) |
Vitamin B12-responsive methylmalonic acidemia | (Orphanet:28) |
Vitamin B12-responsive methylmalonic acidemia type cblA | (Orphanet:79310) |
Vitamin B12-responsive methylmalonic acidemia type cblB | (Orphanet:79311) |
WT limb-blood syndrome | (Orphanet:3466) |
Wilson disease | (Orphanet:905) |