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Diseases
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Name
Orphanumber
Description
XREF(s)
Acute myeloid leukemia with t(6;9)(p23;q34)
402014
A rare subtype of acute myeloid…
Orphanet
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
370026
A distinct form of Acute myeloid…
Orphanet
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
102724
A rare acute myeloid leukemia with…
Orphanet
Acute myeloid leukemia with t(9;11)(p22;q23)
402017
A tumor of hematopoietic and lymphoid…
Orphanet
Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
98829
A rare acute myeloid leukemia (AML)…
Orphanet
,
ICD-10
Acute myeloid leukemia with CEBPA somatic mutations
319480
A subtype of acute myeloid leukemia…
Orphanet
,
OMIM
,
ICD-10
Acute myeloid leukemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2)
402020
A subtype of acute myeloid leukemia…
Orphanet
,
ICD-10
Acute myeloid leukemia with minimal differentiation
98832
A rare subtype of acute myeloid…
Orphanet
,
ICD-10
Acute myeloid leukemia with NPM1 somatic mutations
402026
A subtype of acute myeloid leukemia…
Orphanet
Acute necrotizing encephalopathy of childhood
263524
A rare neurologic disease characterized…
Orphanet
,
ICD-10
,
OMIM
Acute neonatal citrullinemia type I
247546
A severe form of citrullinemia type 1…
Orphanet
Acute promyelocytic leukemia
520
An aggressive form of acute myeloid…
Orphanet
,
MedDRA
,
OMIM
,
MeSH
,
ICD-10
Acute undifferentiated leukemia
98835
A rare acute leukemia of ambiguous…
Orphanet
,
MedDRA
,
ICD-10
,
OMIM
Acyl-CoA dehydrogenase 9 deficiency
99901
A rare disorder characterized by…
Orphanet
,
OMIM
,
ICD-10
ACys amyloidosis
100008
A form of hereditary cerebral…
Orphanet
,
ICD-10
,
ICD-10
,
OMIM
Adams-Oliver syndrome
974
A rare disorder characterized by the…
Orphanet
,
ICD-10
,
MeSH
,
OMIM
,
OMIM
,
OMIM
,
OMIM
,
OMIM
,
OMIM
ADan amyloidosis
97346
A rare, neurodegenerative disease…
Orphanet
,
MeSH
,
OMIM
,
ICD-10
,
ICD-10
Adenine phosphoribosyltransferase deficiency
976
A rare genetic nephropathy secondary to…
Orphanet
,
ICD-10
,
OMIM
Adenocarcinoma of ovary
213504
Orphanet
,
ICD-10
,
MedDRA
Adenosine monophosphate deaminase deficiency
45
A rare metabolic disorder for which two…
Orphanet
,
OMIM
,
OMIM
,
MeSH
,
ICD-10
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