MCID: ATS085

Autosomal Codominant Severe Lipodystrophic Laminopathy malady

Skin diseases, Endocrine diseases, Rare diseases categories

Aliases & Classifications for Autosomal Codominant Severe Lipodystrophic Laminopathy

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Sources:
48Orphanet, 26ICD10 via Orphanet
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Aliases & Descriptions for Autosomal Codominant Severe Lipodystrophic Laminopathy:

Name: Autosomal Codominant Severe Lipodystrophic Laminopathy 48


Classifications:



Characteristics (Orphanet epidemiological data):

48
autosomal codominant severe lipodystrophic laminopathy:
Inheritance: Autosomal dominant; Prevalence: <1/1000000 (Worldwide); Age of onset: Adult


External Ids:

Orphanet48 280365
ICD10 via Orphanet26 E88.1

Summaries for Autosomal Codominant Severe Lipodystrophic Laminopathy

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MalaCards based summary: Autosomal Codominant Severe Lipodystrophic Laminopathy An important gene associated with Autosomal Codominant Severe Lipodystrophic Laminopathy is LMNA (lamin A/C). Affiliated tissues include skin.

Related Diseases for Autosomal Codominant Severe Lipodystrophic Laminopathy

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Symptoms for Autosomal Codominant Severe Lipodystrophic Laminopathy

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Drugs & Therapeutics for Autosomal Codominant Severe Lipodystrophic Laminopathy

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Drug clinical trials:

Search ClinicalTrials for Autosomal Codominant Severe Lipodystrophic Laminopathy

Search NIH Clinical Center for Autosomal Codominant Severe Lipodystrophic Laminopathy

Genetic Tests for Autosomal Codominant Severe Lipodystrophic Laminopathy

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Anatomical Context for Autosomal Codominant Severe Lipodystrophic Laminopathy

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MalaCards organs/tissues related to Autosomal Codominant Severe Lipodystrophic Laminopathy:

31
Skin

Animal Models for Autosomal Codominant Severe Lipodystrophic Laminopathy or affiliated genes

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Publications for Autosomal Codominant Severe Lipodystrophic Laminopathy

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Variations for Autosomal Codominant Severe Lipodystrophic Laminopathy

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Expression for genes affiliated with Autosomal Codominant Severe Lipodystrophic Laminopathy

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Search GEO for disease gene expression data for Autosomal Codominant Severe Lipodystrophic Laminopathy.

Pathways for genes affiliated with Autosomal Codominant Severe Lipodystrophic Laminopathy

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Compounds for genes affiliated with Autosomal Codominant Severe Lipodystrophic Laminopathy

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GO Terms for genes affiliated with Autosomal Codominant Severe Lipodystrophic Laminopathy

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Sources for Autosomal Codominant Severe Lipodystrophic Laminopathy

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2CDC
12ExPASy
13FDA
14FMA
22GTR
23HGMD
24HMDB
25ICD10
26ICD10 via Orphanet
27ICD9CM
28IUPHAR
29KEGG
33MeSH
34MESH via Orphanet
35MGI
38NCI
39NCIt
40NDF-RT
43NINDS
44Novoseek
46OMIM
47OMIM via Orphanet
51PubMed
52QIAGEN
57SNOMED-CT via Orphanet
61UMLS
62UMLS via Orphanet