MCID: PRG037

Progeroid Laminopathies malady

Genetic diseases (common) category

Summaries for Progeroid Laminopathies

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MalaCards based summary: Progeroid Laminopathies An important gene associated with Progeroid Laminopathies is LMNA (lamin A/C).

Aliases & Classifications for Progeroid Laminopathies

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Progeroid Laminopathies, Aliases & Descriptions:

Name: Progeroid Laminopathies 22


Classifications:

Malacards categories (disease lists): (See all malacards categories)
Global: Genetic diseases (common)


Related Diseases for Progeroid Laminopathies

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Symptoms for Progeroid Laminopathies

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Drugs & Therapeutics for Progeroid Laminopathies

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Drug clinical trials:

Search ClinicalTrials for Progeroid Laminopathies

Search NIH Clinical Center for Progeroid Laminopathies

Genetic Tests for Progeroid Laminopathies

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Genetic tests related to Progeroid Laminopathies:

id Genetic test Affiliating Genes
1 Progeroid Laminopathies22 LMNA

Anatomical Context for Progeroid Laminopathies

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Animal Models for Progeroid Laminopathies or affiliated genes

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Publications for Progeroid Laminopathies

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Articles related to Progeroid Laminopathies:

idTitleAuthorsYear
1
Progeroid laminopathy with restrictive dermopathy-like features caused by an isodisomic LMNA mutation p.R435C. (23804595)
2013

Variations for Progeroid Laminopathies

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Expression for genes affiliated with Progeroid Laminopathies

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Search GEO for disease gene expression data for Progeroid Laminopathies.

Pathways for genes affiliated with Progeroid Laminopathies

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Compounds for genes affiliated with Progeroid Laminopathies

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GO Terms for genes affiliated with Progeroid Laminopathies

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Products for genes affiliated with Progeroid Laminopathies

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  • Antibodies
  • Proteins
  • Lysates
  • Antibodies
  • Proteins
  • Kits and Assays

Sources for Progeroid Laminopathies

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4CDC
15ExPASy
16FMA
24GTR
25HGMD
26HMDB
27ICD10
28ICD10 via Orphanet
29ICD9CM
30IUPHAR
31KEGG
35MeSH
36MESH via Orphanet
37MGI
40NCIt
41NDF-RT
44NINDS
45Novoseek
47OMIM
48OMIM via Orphanet
52PubMed
53QIAGEN
58SNOMED-CT via Orphanet
62UMLS
63UMLS via Orphanet