MCID: ATS085

Autosomal Codominant Severe Lipodystrophic Laminopathy malady

Skin diseases, Endocrine diseases, Rare diseases categories
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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.

Aliases & Classifications for Autosomal Codominant Severe Lipodystrophic Laminopathy

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

Name: Autosomal Codominant Severe Lipodystrophic Laminopathy 48


Classifications:

Malacards categories (disease lists): (See all malacards categories)
Global: Rare diseases
Anatomical: Skin diseases, Endocrine diseases


Characteristics (Orphanet epidemiological data):

48
autosomal codominant severe lipodystrophic laminopathy:
Inheritance: Autosomal dominant; Prevalence: <1/1000000; Age of onset: Adulthood


External Ids:

ICD10 via Orphanet26 E88.1

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:

32
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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Expression patterns in normal tissues for genes affiliated with Autosomal Codominant Severe Lipodystrophic Laminopathy

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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Products for genes affiliated with Autosomal Codominant Severe Lipodystrophic Laminopathy

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  • Antibodies
  • Proteins
  • Lysates

Sources for Autosomal Codominant Severe Lipodystrophic Laminopathy

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3CDC
13ExPASy
14FMA
22GTR
23HGMD
24HMDB
25ICD10
26ICD10 via Orphanet
27ICD9CM
28IUPHAR
29KEGG
34MeSH
35MESH via Orphanet
36MGI
39NCIt
40NDF-RT
43NINDS
44Novoseek
46OMIM
47OMIM via Orphanet
51PubMed
52QIAGEN
58SNOMED-CT via Orphanet
62UMLS
63UMLS via Orphanet