Neutropenia
Symptom Information:
Symptom ID: | HPO:0001875 | ||||||||||||||||||||||||
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 leukocytes(HPO:0001881) Abnormality of myeloid leukocytes(HPO:0010974) Abnormality of granulocytes(HPO:0001911) Abnormality of neutrophils(HPO:0001874) Abnormal neutrophil cell number(HPO:0011991) Neutropenia(HPO:0001875) Abnormality of the immune system(HPO:0002715) Abnormality of cellular immune system(HPO:0010987) Abnormality of leukocytes(HPO:0001881) Abnormality of myeloid leukocytes(HPO:0010974) Abnormality of granulocytes(HPO:0001911) Abnormality of neutrophils(HPO:0001874) Abnormal neutrophil cell number(HPO:0011991) Neutropenia(HPO:0001875) MedDRA: Blood and lymphatic system disorders(MedDRA:10005329) Abnormality of leukocytes(HPO:0001881) Neutropenia(HPO:0001875) Investigations(MedDRA:10022891) Haematology investigations (incl blood groups)(MedDRA:10018851) White blood cell analyses(MedDRA:10047938) Neutropenia(HPO:0001875) |
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Database Frequency: | 83 / 7739 | ||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
3-@METHYLGLUTACONIC ACIDURIA WITH CATARACTS, NEUROLOGIC INVOLVEMENT,AND NEUTROPENIA | (OMIM:616271) |
AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE | (OMIM:601495) |
AGAMMAGLOBULINEMIA 3, AUTOSOMAL RECESSIVE | (OMIM:613501) |
AGAMMAGLOBULINEMIA 4, AUTOSOMAL RECESSIVE | (OMIM:613502) |
AGAMMAGLOBULINEMIA 7, AUTOSOMAL RECESSIVE | (OMIM:615214) |
Adult idiopathic neutropenia | (Orphanet:2688) |
Aspartylglucosaminuria | (Orphanet:93) |
Autosomal agammaglobulinemia | (Orphanet:33110) |
Autosomal dominant severe congenital neutropenia | (Orphanet:486) |
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | (Orphanet:331176) |
Barth syndrome | (Orphanet:111) |
Blackfan-Diamond anemia | (Orphanet:124) |
COMBINED INFLAMMATORY AND IMMUNOLOGIC DEFECT | (OMIM:216920) |
Cartilage-hair hypoplasia | (Orphanet:175) |
Cohen syndrome | (Orphanet:193) |
Combined immunodeficiency due to STK4 deficiency | (Orphanet:314689) |
DIAMOND-BLACKFAN ANEMIA 11 | (OMIM:614900) |
DK1-CDG | (Orphanet:91131) |
ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNELDEFICIENCY | (OMIM:614520) |
ENTEROPATHY, FAMILIAL, WITH VILLOUS EDEMA AND IMMUNOGLOBULIN G2 DEFICIENCY | (OMIM:600351) |
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 G | (OMIM:614082) |
Familial isolated dilated cardiomyopathy | (Orphanet:154) |
Fanconi anemia | (Orphanet:84) |
Felty syndrome | (Orphanet:47612) |
Glutathione synthetase deficiency with 5-oxoprolinuria | (Orphanet:289846) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type b | (Orphanet:79259) |
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 4 | (OMIM:603552) |
Hereditary folate malabsorption | (Orphanet:90045) |
Hermansky-Pudlak syndrome | (Orphanet:79430) |
Hermansky-Pudlak syndrome with neutropenia | (Orphanet:183678) |
Hyper-IgM syndrome type 3 | (Orphanet:101090) |
IMMUNODEFICIENCY 23 | (OMIM:615816) |
IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY | (OMIM:614700) |
Immunodeficiency by defective expression of HLA class 2 | (Orphanet:572) |
Kostmann syndrome | (Orphanet:99749) |
LAZY LEUKOCYTE SYNDROME | (OMIM:150550) |
LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA | (OMIM:608809) |
Letterer-Siwe disease | (Orphanet:99870) |
Lichstenstein syndrome | (Orphanet:2390) |
MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,AND PSYCHOMOTOR DELAY | (OMIM:601347) |
Methylmalonic acidemia with homocystinuria | (Orphanet:26) |
Methylmalonic acidemia with homocystinuria, type cblC | (Orphanet:79282) |
Methylmalonic acidemia with homocystinuria, type cblF | (Orphanet:79284) |
Methylmalonic acidemia with homocystinuria, type cblJ | (Orphanet:369955) |
Microcephalic primordial dwarfism, Toriello type | (Orphanet:2643) |
Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies | (Orphanet:369897) |
Monocytopenia with susceptibility to infections | (Orphanet:228423) |
Myopathy, lactic acidosis, and sideroblastic anemia 2; MLASA2 | (OMIM:613561) |
NEUTROPENIA, CHRONIC FAMILIAL | (OMIM:162700) |
NEUTROPENIA, SEVERE CONGENITAL, 6, AUTOSOMAL RECESSIVE | (OMIM:616022) |
ONYCHOTRICHODYSPLASIA AND NEUTROPENIA | (OMIM:258360) |
PELGER-HUET ANOMALY | (OMIM:169400) |
Pearson syndrome | (Orphanet:699) |
Poikiloderma with neutropenia | (Orphanet:221046) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Primary immunodeficiency syndrome due to p14 deficiency | (Orphanet:90023) |
Propionic acidemia | (Orphanet:35) |
RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER | (OMIM:614470) |
RETINAL VENOUS BEADING | (OMIM:180080) |
Recurrent infections-myelofibrosis-nephromegaly syndrome | (Orphanet:369852) |
SLC35A1-CDG | (Orphanet:238459) |
Schimke immuno-osseous dysplasia | (Orphanet:1830) |
Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |
Shwachman-Diamond syndrome | (Orphanet:811) |
THROMBOCYTOPENIA 5 | (OMIM:616216) |
THROMBOCYTOPENIA, CYCLIC | (OMIM:188020) |
TRIMETHYLAMINURIA | (OMIM:602079) |
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) |
WHIM syndrome | (Orphanet:51636) |
Wolcott-Rallison syndrome | (Orphanet:1667) |
Wolfram syndrome, mitochondrial form | (OMIM:598500) |
X-linked dyserythropoetic anemia with abnormal platelets and neutropenia | (Orphanet:363727) |
X-linked hyper-IgM syndrome | (Orphanet:101088) |
[DEL] GLYCOGEN STORAGE DISEASE Ib | (OMIM:232220) |
[DEL] NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4 | (OMIM:612541) |