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CDKL5 deficiency disorder
rare X-linked genetic disorder
CDKL5 Deficiency
DEE2
Developmental and epileptic encephalopathy-2
CDKL5 Disorder
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Statements
instance of
class of disease
0 references
subclass of
developmental and epileptic encephalopathy
0 references
genetic association
CDKL5
0 references
Identifiers
GARD rare disease ID
12173
0 references
ICD-10
G40.4
0 references
Medical Dictionary for Regulatory Activities ID
10071352
1 reference
reference URL
https://cdn.who.int/media/docs/default-source/classification/icd/icd-10/icd-10-to-meddra-map---june-2023---codes-mapping.xlsx
based on heuristic
inferred by common ICD-10 mappings on Wikidata and on source
OMIM ID
300672
0 references
Orphanet ID
505652
0 references
UMLS CUI
CL494907
0 references
C4750718
1 reference
based on heuristic
inferred by common Orphanet mappings on source and on Wikidata
stated in
UMLS 2023
retrieved
16 June 2023
WikiProjectMed ID
CDKL5 deficiency disorder
0 references
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(1 entry)
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enwiki
CDKL5 deficiency disorder
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