MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen

Acute motor axonal neuropathy

ORPHA:98918Kr.
Multigenic/multifactorial, Not applicable

Acute myeloblastic leukemia with maturation

ORPHA:98834Kr.
Not applicable

Acute myeloblastic leukemia without maturation

ORPHA:98833Kr.
Not applicable

Acute myeloid leukaemia with myelodysplasia-related features

ORPHA:86845Kr.
Not applicable

Acute myeloid leukemia

ORPHA:519Kl. gruppe

Acute myeloid leukemia and myelodysplastic syndromes related to radiation

ORPHA:164726Kr.

Acute myeloid leukemia with 11q23 abnormalities

ORPHA:98831Kr.

Acute myeloid leukemia with CEBPA somatic mutations

ORPHA:319480Kr.
Not applicable

Acute myeloid leukemia with NPM1 somatic mutations

ORPHA:402026Kr.
Not applicable

Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)

ORPHA:98829Kr.

Acute myeloid leukemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2)

ORPHA:402020Kr.

Acute myeloid leukemia with minimal differentiation

ORPHA:98832Kr.
Not applicable

Acute myeloid leukemia with recurrent genetic anomaly

ORPHA:98277Kat.

Acute myeloid leukemia with t(6;9)(p23;q34)

ORPHA:402014Kr.

Acute myeloid leukemia with t(8;16)(p11;p13) translocation

ORPHA:370026Kr.
Not applicable

Acute myeloid leukemia with t(8;21)(q22;q22) translocation

ORPHA:102724Kr.

Acute myeloid leukemia with t(9;11)(p22;q23)

ORPHA:402017Kr.

Acute myeloid leukemia with t(9;22)(q34.1;q11.2)

ORPHA:585867Kr.

Acute myelomonocytic leukemia

ORPHA:517Kr.
Not applicable

Acute necrotizing encephalopathy of childhood

ORPHA:263524Kr.
Not applicable

Acute neonatal citrullinemia type I

ORPHA:247546Kl. subt.
Autosomal recessive

Acute opioid intoxication

ORPHA:35889Kr.
Not applicable

Acute pandysautonomia

ORPHA:231457Kr.
Multigenic/multifactorial, Not applicable

Acute panmyelosis with myelofibrosis

ORPHA:86843Kr.
Not applicable