MCID: SPN269
MIFTS: 5

Spondylometaphyseal Dysplasia, Czarny-Ratajczak Type

Categories: Bone diseases, Fetal diseases, Rare diseases

Aliases & Classifications for Spondylometaphyseal Dysplasia, Czarny-Ratajczak Type

MalaCards integrated aliases for Spondylometaphyseal Dysplasia, Czarny-Ratajczak Type:

Name: Spondylometaphyseal Dysplasia, Czarny-Ratajczak Type 58

Characteristics:

Orphanet epidemiological data:

58
spondylometaphyseal dysplasia, czarny-ratajczak type
Prevalence: <1/1000000 (Worldwide); Age of onset: Infancy,Neonatal;

Classifications:

Orphanet: 58  
Rare bone diseases
Developmental anomalies during embryogenesis


External Ids:

ICD10 via Orphanet 33 Q77.8
Orphanet 58 ORPHA370019

Summaries for Spondylometaphyseal Dysplasia, Czarny-Ratajczak Type

MalaCards based summary : Spondylometaphyseal Dysplasia, Czarny-Ratajczak Type Affiliated tissues include bone.

Related Diseases for Spondylometaphyseal Dysplasia, Czarny-Ratajczak Type

Symptoms & Phenotypes for Spondylometaphyseal Dysplasia, Czarny-Ratajczak Type

Drugs & Therapeutics for Spondylometaphyseal Dysplasia, Czarny-Ratajczak Type

Search Clinical Trials , NIH Clinical Center for Spondylometaphyseal Dysplasia, Czarny-Ratajczak Type

Genetic Tests for Spondylometaphyseal Dysplasia, Czarny-Ratajczak Type

Anatomical Context for Spondylometaphyseal Dysplasia, Czarny-Ratajczak Type

MalaCards organs/tissues related to Spondylometaphyseal Dysplasia, Czarny-Ratajczak Type:

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Bone

Publications for Spondylometaphyseal Dysplasia, Czarny-Ratajczak Type

Variations for Spondylometaphyseal Dysplasia, Czarny-Ratajczak Type

Expression for Spondylometaphyseal Dysplasia, Czarny-Ratajczak Type

Search GEO for disease gene expression data for Spondylometaphyseal Dysplasia, Czarny-Ratajczak Type.

Pathways for Spondylometaphyseal Dysplasia, Czarny-Ratajczak Type

GO Terms for Spondylometaphyseal Dysplasia, Czarny-Ratajczak Type

Sources for Spondylometaphyseal Dysplasia, Czarny-Ratajczak Type

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
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
43 MeSH
44 MESH via Orphanet
45 MGI
48 NCI
49 NCIt
50 NDF-RT
53 NINDS
54 Novoseek
56 OMIM
57 OMIM via Orphanet
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 TGDB
70 Tocris
71 UMLS
72 UMLS via Orphanet
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