MCID: FML138

Familial Myelodysplasia malady

Genetic diseases (common) category

Aliases & Classifications for Familial Myelodysplasia

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Aliases & Descriptions for Familial Myelodysplasia:

Name: Familial Myelodysplasia 20


Classifications:



Summaries for Familial Myelodysplasia

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MalaCards based summary: Familial Myelodysplasia An important gene associated with Familial Myelodysplasia is RUNX1 (runt-related transcription factor 1). Affiliated tissues include myeloid.

Related Diseases for Familial Myelodysplasia

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Symptoms for Familial Myelodysplasia

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Drugs & Therapeutics for Familial Myelodysplasia

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Drug clinical trials:

Search ClinicalTrials for Familial Myelodysplasia

Search NIH Clinical Center for Familial Myelodysplasia

Genetic Tests for Familial Myelodysplasia

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Genetic tests related to Familial Myelodysplasia:

id Genetic test Affiliating Genes
1 Familial Myelodysplasia20

Anatomical Context for Familial Myelodysplasia

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MalaCards organs/tissues related to Familial Myelodysplasia:

31
Myeloid

Animal Models for Familial Myelodysplasia or affiliated genes

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Publications for Familial Myelodysplasia

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Articles related to Familial Myelodysplasia:

idTitleAuthorsYear
1
Marked genetic heterogeneity in familial myelodysplasia/acute myeloid leukaemia. (22533337)
2012
2
Familial myelodysplasia and acute myeloid leukaemia--a review. (18173751)
2008
3
Familial myelodysplasia. (2507067)
1989
4
Familial myelodysplasia: progressive disease associated with emergency of monosomy 7. (3567084)
1987

Variations for Familial Myelodysplasia

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Expression for genes affiliated with Familial Myelodysplasia

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Search GEO for disease gene expression data for Familial Myelodysplasia.

Pathways for genes affiliated with Familial Myelodysplasia

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Compounds for genes affiliated with Familial Myelodysplasia

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GO Terms for genes affiliated with Familial Myelodysplasia

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Sources for Familial Myelodysplasia

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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