Blood Diseases | Page 1

335 diseases found in 4 pages

5 Diseases

5q- syndrome

A Diseases

Aagenaes syndrome Abdominal aortic aneurysm Abetalipoproteinemia Acatalasemia Aceruloplasminemia Acquired agranulocytosis Acquired hemophilia Acquired hemophilia A Acquired pure red cell aplasia Acquired Von Willebrand syndrome Acute erythroid leukemia Acute graft versus host disease Acute monoblastic leukemia Acute myeloblastic leukemia with maturation Acute myeloblastic leukemia without maturation Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22) Acute myeloid leukemia with inv3(p21;q26.2) or t(3;3)(p21;q26.2) Acute myelomonocytic leukemia Acute panmyelosis with myelofibrosis Acute promyelocytic leukemia Adenosine Deaminase 2 deficiency Adrenocortical carcinoma Adult T-cell leukemia/lymphoma Afibrinogenemia ALK+ histiocytosis Alpha-thalassemia x-linked intellectual disability syndrome AML with myelodysplasia-related features Anemia due to Adenosine triphosphatase deficiency Anemia sideroblastic and spinocerebellar ataxia Aneurysm of sinus of Valsalva Angioimmunoblastic T-cell lymphoma Angioma hereditary neurocutaneous Angioma serpiginosum Angiosarcoma Antiphospholipid syndrome Aplasia cutis congenita intestinal lymphangiectasia Aplastic anemia Arterial calcification of infancy Arterial tortuosity syndrome Atransferrinemia Atypical hemolytic uremic syndrome Autoimmune lymphoproliferative syndrome Autosomal recessive protein C deficiency

B Diseases

Bannayan-Riley-Ruvalcaba syndrome Behçet disease Beta-thalassemia Blastic plasmacytoid dendritic cell Bleeding disorder due to P2RY12 defect Bloom syndrome Blue rubber bleb nevus syndrome Buerger disease Burkitt lymphoma

C Diseases

Campomelia Cumming type Castleman disease Cerebral cavernous malformation Chediak-Higashi syndrome Chromosome 17q11.2 deletion syndrome Chronic lymphocytic leukemia Chronic myeloid leukemia Chylous ascites CLOVES syndrome Cobb syndrome Cold agglutinin disease Congenital amegakaryocytic thrombocytopenia Congenital analbuminemia Congenital dyserythropoietic anemia type 1 Congenital dyserythropoietic anemia type 2 Congenital dyserythropoietic anemia type 3 Congenital erythropoietic porphyria Congenital myasthenic syndrome with episodic apnea Congenital pulmonary lymphangiectasia Congenital thrombotic thrombocytopenic purpura Cutaneous mastocytoma Cutis laxa, autosomal recessive type 1 Cutis marmorata telangiectatica congenita Cyclic neutropenia Cyclic thrombocytopenia Cystic medial necrosis of aorta

D Diseases

Dahlberg Borer Newcomer syndrome Deafness-lymphedema-leukemia syndrome Dehydrated hereditary stomatocytosis Diamond-Blackfan anemia Diamond-Blackfan anemia 2 Diamond-Blackfan anemia 3 Dysfibrinogenemia Dyskeratosis congenita Dyskeratosis congenita autosomal dominant Dyskeratosis congenita autosomal recessive Dyskeratosis congenita X-linked

E Diseases

Ehlers-Danlos syndrome, dysfibronectinemic type Eosinophilic granulomatosis with polyangiitis Erythema elevatum diutinum Essential thrombocythemia Evans syndrome Extranodal nasal NK/T cell lymphoma

F Diseases

Fabry disease Factor V deficiency Factor VII deficiency Factor V Leiden thrombophilia

The RareGuru disease database is regularly updated using data generously provided by GARD, the United States Genetic and Rare Disease Information Center.

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