MCID: ATS085

Autosomal Codominant Severe Lipodystrophic Laminopathy malady

Skin diseases, Endocrine diseases, Rare diseases categories

Summaries for Autosomal Codominant Severe Lipodystrophic Laminopathy

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34MalaCards
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MalaCards: 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:
50Orphanet, 27ICD10 via Orphanet
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Classifications:

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


Characteristics (Orphanet epidemiological data):

50
autosomal codominant severe lipodystrophic laminopathy:
Inheritance: Autosomal dominant; Prevalence: <1/1000000; Age of onset: Adulthood


Aliases & Descriptions:

autosomal codominant severe lipodystrophic laminopathy 50


External Ids:

ICD10 via Orphanet27 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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Sources:
6CenterWatch, 43NIH Clinical Center, 7ClinicalTrials
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Approved drugs:

Search CenterWatch for Autosomal Codominant Severe Lipodystrophic Laminopathy

Drug clinical trials:

Search ClinicalTrials for Autosomal Codominant Severe Lipodystrophic Laminopathy

Search NIH Clinical Center for Autosomal Codominant Severe Lipodystrophic Laminopathy

Search CenterWatch 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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34MalaCards
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MalaCards organs/tissues related to Autosomal Codominant Severe Lipodystrophic Laminopathy:

34
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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Sources:
2BioGPS, 16Gene Expression Omnibus DataSets
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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
  • Antibodies

Sources for Autosomal Codominant Severe Lipodystrophic Laminopathy

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4CDC
14ExPASy
15FMA
23GTR
24HGMD
25HMDB
26ICD10
27ICD10 via Orphanet
28ICD9CM
30IUPHAR
31KEGG
36MeSH
37MESH via Orphanet
38MGI
41NCIt
42NDF-RT
45NINDS
46Novoseek
48OMIM
49OMIM via Orphanet
53PubMed
54QIAGEN
60SNOMED-CT via Orphanet
63UMLS
64UMLS via Orphanet