DALD
MCID: DNZ002
MIFTS: 14

Dianzani Autoimmune Lymphoproliferative Disease (DALD)

Categories: Blood diseases, Immune diseases, Rare diseases

Aliases & Classifications for Dianzani Autoimmune Lymphoproliferative Disease

MalaCards integrated aliases for Dianzani Autoimmune Lymphoproliferative Disease:

Name: Dianzani Autoimmune Lymphoproliferative Disease 57 58 54
Dianzani Autoimmune Lymphoproliferative Syndrome 20 70
Dald 57 58
Autoimmune Lymphoproliferative Syndrome Without Fas Mutations 20
Dianzani Form of Autoimmune Lymphoproliferative Disease 20

Characteristics:

Orphanet epidemiological data:

58
dianzani autoimmune lymphoproliferative disease
Prevalence: <1/1000000 (Worldwide); Age of onset: All ages;

Classifications:

Orphanet: 58  
Rare immunological diseases


External Ids:

OMIM® 57 605233
ICD10 via Orphanet 33 D47.9
UMLS via Orphanet 71 C2931071
Orphanet 58 ORPHA275523
UMLS 70 C2931071

Summaries for Dianzani Autoimmune Lymphoproliferative Disease

MalaCards based summary : Dianzani Autoimmune Lymphoproliferative Disease, is also known as dianzani autoimmune lymphoproliferative syndrome. An important gene associated with Dianzani Autoimmune Lymphoproliferative Disease is FAS (Fas Cell Surface Death Receptor). Affiliated tissues include t cells.

More information from OMIM: 605233

Related Diseases for Dianzani Autoimmune Lymphoproliferative Disease

Symptoms & Phenotypes for Dianzani Autoimmune Lymphoproliferative Disease

Clinical features from OMIM®:

605233 (Updated 05-Apr-2021)

Drugs & Therapeutics for Dianzani Autoimmune Lymphoproliferative Disease

Search Clinical Trials , NIH Clinical Center for Dianzani Autoimmune Lymphoproliferative Disease

Genetic Tests for Dianzani Autoimmune Lymphoproliferative Disease

Anatomical Context for Dianzani Autoimmune Lymphoproliferative Disease

MalaCards organs/tissues related to Dianzani Autoimmune Lymphoproliferative Disease:

40
T Cells

Publications for Dianzani Autoimmune Lymphoproliferative Disease

Articles related to Dianzani Autoimmune Lymphoproliferative Disease:

# Title Authors PMID Year
1
Variations of the perforin gene in patients with autoimmunity/lymphoproliferation and defective Fas function. 61 57
16720836 2006
2
Deficiency of the Fas apoptosis pathway without Fas gene mutations is a familial trait predisposing to development of autoimmune diseases and cancer. 57
10807785 2000
3
Deficiency of the Fas apoptosis pathway without Fas gene mutations in pediatric patients with autoimmunity/lymphoproliferation. 57
9108407 1997
4
The broad spectrum of autoimmune lymphoproliferative disease: molecular bases, clinical features and long-term follow-up in 31 patients. 54 61
16537120 2006
5
Association of severe myoclonic epilepsy of infancy (SMEI) with probable autoimmune lymphoproliferative syndrome-variant. 61
25669891 2014
6
IL-17 protects T cells from apoptosis and contributes to development of ALPS-like phenotypes. 61
24363402 2014
7
Variations of the UNC13D gene in patients with autoimmune lymphoproliferative syndrome. 61
23840885 2013
8
The -346T polymorphism of the SH2D1A gene is a risk factor for development of autoimmunity/lymphoproliferation in males with defective Fas function. 61
22425739 2012
9
High levels of osteopontin associated with polymorphisms in its gene are a risk factor for development of autoimmunity/lymphoproliferation. 61
14592838 2004

Variations for Dianzani Autoimmune Lymphoproliferative Disease

Expression for Dianzani Autoimmune Lymphoproliferative Disease

Search GEO for disease gene expression data for Dianzani Autoimmune Lymphoproliferative Disease.

Pathways for Dianzani Autoimmune Lymphoproliferative Disease

GO Terms for Dianzani Autoimmune Lymphoproliferative Disease

Sources for Dianzani Autoimmune Lymphoproliferative Disease

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-Apr-2021)
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 Tocris
70 UMLS
71 UMLS via Orphanet
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