MCID: FML317
MIFTS: 6

Familial Monosomy 7 Syndrome

Categories: Blood diseases, Eye diseases, Fetal diseases, Genetic diseases, Rare diseases

Aliases & Classifications for Familial Monosomy 7 Syndrome

MalaCards integrated aliases for Familial Monosomy 7 Syndrome:

Name: Familial Monosomy 7 Syndrome 58

Classifications:

Orphanet: 58  
Rare haematological diseases


External Ids:

Orphanet 58 ORPHA495930

Summaries for Familial Monosomy 7 Syndrome

MalaCards based summary : Familial Monosomy 7 Syndrome is related to myelodysplastic syndrome. An important gene associated with Familial Monosomy 7 Syndrome is SAMD9L (Sterile Alpha Motif Domain Containing 9 Like).

Related Diseases for Familial Monosomy 7 Syndrome

Diseases in the Autosomal Monosomy family:

Monosomy 21 Familial Monosomy 7 Syndrome
Monosomy 9q22.3 Total Autosomal Monosomy
Monosomy 22

Diseases related to Familial Monosomy 7 Syndrome via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 myelodysplastic syndrome 10.0

Symptoms & Phenotypes for Familial Monosomy 7 Syndrome

Drugs & Therapeutics for Familial Monosomy 7 Syndrome

Search Clinical Trials , NIH Clinical Center for Familial Monosomy 7 Syndrome

Genetic Tests for Familial Monosomy 7 Syndrome

Anatomical Context for Familial Monosomy 7 Syndrome

Publications for Familial Monosomy 7 Syndrome

Articles related to Familial Monosomy 7 Syndrome:

# Title Authors PMID Year
1
Familial Monosomy 7 Syndrome Associated with Myelodysplasia. 61
31209763 2019
2
Familial Monosomy 7 Syndrome ─ RETIRED CHAPTER, FOR HISTORICAL REFERENCE ONLY 61
20614583 2010

Variations for Familial Monosomy 7 Syndrome

Expression for Familial Monosomy 7 Syndrome

Search GEO for disease gene expression data for Familial Monosomy 7 Syndrome.

Pathways for Familial Monosomy 7 Syndrome

GO Terms for Familial Monosomy 7 Syndrome

Sources for Familial Monosomy 7 Syndrome

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
20 GARD
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
53 NINDS
54 Novoseek
56 OMIM via Orphanet
57 OMIM® (Updated 05-Mar-2021)
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 TGDB
70 Tocris
71 UMLS
72 UMLS via Orphanet
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