CDKL5 deficiency disorder
rare X-linked genetic disorder
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CDKL5 deficiency disorder
Summary
CDKL5 deficiency disorder is a class of disease[1]. It draws 6 Wikipedia views per month (class_of_disease category, ranking #631 of 1,968).[2]
Key Facts
- CDKL5 deficiency disorder's instance of is recorded as class of disease[3].
- CDKL5 deficiency disorder's subclass of is recorded as developmental and epileptic encephalopathy[4].
- CDKL5 deficiency disorder's OMIM ID is recorded as 300672[5].
- CDKL5 deficiency disorder's ICD-10 ID is recorded as G40.4[6].
- CDKL5 deficiency disorder's Orphanet ID is recorded as 505652[7].
- CDKL5 deficiency disorder's genetic association is recorded as CDKL5[8].
- CDKL5 deficiency disorder's UMLS CUI is recorded as CL494907[9].
- CDKL5 deficiency disorder's UMLS CUI is recorded as C4750718[10].
- CDKL5 deficiency disorder's Medical Dictionary for Regulatory Activities ID is recorded as 10071352[11].
- CDKL5 deficiency disorder's GARD rare disease ID is recorded as 12173[12].
- CDKL5 deficiency disorder's WikiProjectMed ID is recorded as CDKL5 deficiency disorder[13].
Why It Matters
CDKL5 deficiency disorder draws 6 Wikipedia views per month (class_of_disease category, ranking #631 of 1,968).[2]