Orphanet · Orphadata CC-BY-4.0
Сирек (орфандық) аурулар
7,547 аурудың толық базасы: генетика, фенотиптер, эпидемиология, препараттар және зерттеулер.
7,547
Аурулар
4 552
Гендер
8 700
Фенотиптер
140
Аймақтар
Все (7,547)Био аномалияСанатКлиникалық топКлиникалық подтипClinical syndromeАуруЭтиологиялық подтипГистопатологиялық подтипМальформацияМорфологиялық аномалияКлиникалық жағдай
Acute motor axonal neuropathy
Multigenic/multifactorial, Not applicable
All ages
Acute myeloblastic leukemia with maturation
Not applicable
All ages
Acute myeloblastic leukemia without maturation
Not applicable
Adult
Acute myeloid leukaemia with myelodysplasia-related features
Not applicable
Adult
Acute myeloid leukemia
All ages
Acute myeloid leukemia and myelodysplastic syndromes related to radiation
Adult, Elderly
Acute myeloid leukemia with 11q23 abnormalities
Childhood
Acute myeloid leukemia with CEBPA somatic mutations
Not applicable
Acute myeloid leukemia with NPM1 somatic mutations
Not applicable
Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
Adult
Acute myeloid leukemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2)
Acute myeloid leukemia with minimal differentiation
Not applicable
Adult
Acute myeloid leukemia with recurrent genetic anomaly
Acute myeloid leukemia with t(6;9)(p23;q34)
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
Not applicable
All ages
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Adolescent, Adult, Childhood
Acute myeloid leukemia with t(9;11)(p22;q23)
Acute myeloid leukemia with t(9;22)(q34.1;q11.2)
Adolescent, Adult, Childhood, Elderly, Infancy, Neonatal
Acute myelomonocytic leukemia
Not applicable
Adult
Acute necrotizing encephalopathy of childhood
Not applicable
Childhood
Acute neonatal citrullinemia type I
Autosomal recessive
Infancy, Neonatal
Acute opioid intoxication
Not applicable
All ages
Acute pandysautonomia
Multigenic/multifactorial, Not applicable
All ages
Acute panmyelosis with myelofibrosis
Not applicable
Adult