Skip to main content
Log in
Sciensano
Support
Belgian Genetic Tests database
Toggle navigation
Main navigation
Home
Genetic tests
Analytes
Diseases
Labs
Guide
Contact
Diseases
20
50
100
Search
Reset
Name
Orphanumber
Description
XREF(s)
Amelocerebrohypohidrotic syndrome
1946
A genetically heterogeneous autosomal…
Orphanet
,
ICD-10
,
OMIM
Amish infantile epilepsy syndrome
171714
Orphanet
,
ICD-10
,
OMIM
Amish lethal microcephaly
99742
A very rare syndrome characterized by…
Orphanet
,
MeSH
,
ICD-10
,
OMIM
Amish nemaline myopathy
98902
A type of nemaline myopathy (NM) only…
Orphanet
,
OMIM
,
ICD-10
AA amyloidosis
85445
A rare amyloidosis that complicates…
Orphanet
,
ICD-10
,
MedDRA
Amyloidosis cutis dyschromia
319635
A rare primary cutaneous amyloidosis…
Orphanet
,
OMIM
,
ICD-10
,
ICD-10
Amyotrophic lateral sclerosis
803
A neurodegenerative disease…
Orphanet
,
OMIM
,
OMIM
,
OMIM
,
OMIM
,
OMIM
,
OMIM
,
MedDRA
,
MeSH
,
ICD-10
,
OMIM
,
OMIM
,
OMIM
,
OMIM
,
OMIM
,
OMIM
,
OMIM
,
OMIM
,
OMIM
,
OMIM
,
OMIM
,
OMIM
,
OMIM
,
OMIM
,
OMIM
,
OMIM
,
OMIM
Amyotrophic lateral sclerosis type 4
357043
A rare, genetic motor neuron disease…
Orphanet
,
OMIM
,
ICD-10
Analysis of the toxicity of enzalutamide
529828
Orphanet
Anaplastic astrocytoma
251589
A rare, high-grade, malignant glial…
Orphanet
,
MedDRA
,
MedDRA
,
ICD-10
Anaplastic oligoastrocytoma
251663
A rare and aggressive glial tumor of…
Orphanet
,
ICD-10
Anaplastic oligodendroglioma
251630
A rare glial tumor characterized by a…
Orphanet
,
MedDRA
,
ICD-10
,
OMIM
,
OMIM
Anauxetic dysplasia
93347
A rare spondyloepimetaphyseal dysplasia…
Orphanet
,
OMIM
,
OMIM
,
MeSH
,
ICD-10
,
OMIM
Andersen-Tawil syndrome
37553
https://www.orpha.net/consor/cgi-bin/Di…
Andersen-Tawil syndrome
37553
A rare disorder characterized by…
Orphanet
,
ICD-10
,
OMIM
ANE syndrome
157954
A rare, genetic, neuro-endocrino-…
Orphanet
,
OMIM
,
ICD-10
Aneurysm-osteoarthritis syndrome
284984
A rare, genetic, systemic disease…
Orphanet
,
ICD-10
,
OMIM
Angelman syndrome
72
Orphanet
Angelman syndrome due to imprinting defect in 15q11-q13
411515
Orphanet
Angelman syndrome due to maternal 15q11q13 deletion
98794
Orphanet
,
ICD-10
Pagination
First page
« First
Previous page
‹ Previous
Page
9
Page
10
Page
11
Page
12
Current page
13
Page
14
Page
15
Page
16
Page
17
Next page
Next ›
Last page
Last »
Download XLSX
Download PDF
Did not find what you were looking for? Contact us through the support center.
Read more