MCID: ATS245
MIFTS: 4

Autosomal Recessive Severe Congenital Neutropenia Due to Cxcr2 Deficiency

Categories: Blood diseases, Rare diseases

Aliases & Classifications for Autosomal Recessive Severe Congenital Neutropenia Due to Cxcr2...

MalaCards integrated aliases for Autosomal Recessive Severe Congenital Neutropenia Due to Cxcr2 Deficiency:

Name: Autosomal Recessive Severe Congenital Neutropenia Due to Cxcr2 Deficiency 58

Characteristics:

Orphanet epidemiological data:

58
autosomal recessive severe congenital neutropenia due to cxcr2 deficiency
Inheritance: Autosomal recessive; Prevalence: <1/1000000 (Worldwide); Age of onset: Infancy,Neonatal;

Classifications:

Orphanet: 58  
Rare immunological diseases


External Ids:

ICD10 via Orphanet 33 D70
Orphanet 58 ORPHA420699

Summaries for Autosomal Recessive Severe Congenital Neutropenia Due to Cxcr2...

MalaCards based summary : Autosomal Recessive Severe Congenital Neutropenia Due to Cxcr2 Deficiency An important gene associated with Autosomal Recessive Severe Congenital Neutropenia Due to Cxcr2 Deficiency is CXCR2 (C-X-C Motif Chemokine Receptor 2).

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Sources for Autosomal Recessive Severe Congenital Neutropenia Due to Cxcr2...

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