infantile parkinsonism-dystonia
Infantile dystonia-parkinsonism (IPD) is an extremely rare inherited neurological syndrome that presents in early infancy with hypokinetic parkinsonism and dystonia and that can be fatal
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infantile parkinsonism-dystonia
Summary
infantile parkinsonism-dystonia is a rare disease[1]. It draws 5 Wikipedia views per month (rare_disease category, ranking #235 of 627).[2]
Key Facts
- infantile parkinsonism-dystonia's instance of is recorded as rare disease[3].
- infantile parkinsonism-dystonia's instance of is recorded as class of disease[4].
- infantile parkinsonism-dystonia's subclass of is recorded as dystonia[5].
- infantile parkinsonism-dystonia's subclass of is recorded as rare parkinsonian syndrome due to genetic neurodegenerative disease[6].
- infantile parkinsonism-dystonia's subclass of is recorded as persistent combined dystonia[7].
- infantile parkinsonism-dystonia's MeSH descriptor ID is recorded as C567730[8].
- infantile parkinsonism-dystonia's OMIM ID is recorded as 613135[9].
- infantile parkinsonism-dystonia's symptoms and signs is recorded as tremor[10].
- infantile parkinsonism-dystonia's symptoms and signs is recorded as dystonia[11].
- infantile parkinsonism-dystonia's medical examination is recorded as genetic testing[12].
- infantile parkinsonism-dystonia's Orphanet ID is recorded as 238455[13].
- infantile parkinsonism-dystonia's NCI Thesaurus ID is recorded as C129866[14].
- infantile parkinsonism-dystonia's genetic association is recorded as SLC6A3[15].
- infantile parkinsonism-dystonia's Google Knowledge Graph ID is recorded as /g/11h75rh1j1[16].
- infantile parkinsonism-dystonia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_238455[17].
- infantile parkinsonism-dystonia's UMLS CUI is recorded as C2751067[18].
- infantile parkinsonism-dystonia's GARD rare disease ID is recorded as 10484[19].
- infantile parkinsonism-dystonia's Mondo ID is recorded as MONDO_0013150[20].
- infantile parkinsonism-dystonia's Genetics Home Reference Conditions ID is recorded as dopamine-transporter-deficiency-syndrome[21].
- infantile parkinsonism-dystonia's WikiProjectMed ID is recorded as Dopamine transporter deficiency syndrome[22].
- infantile parkinsonism-dystonia's UniProt disease ID is recorded as DI-02782[23].
Why It Matters
infantile parkinsonism-dystonia draws 5 Wikipedia views per month (rare_disease category, ranking #235 of 627).[2]