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 59

Characteristics:

Orphanet epidemiological data:

59
spondylometaphyseal dysplasia, czarny-ratajczak type
Prevalence: <1/1000000 (Worldwide); Age of onset: Infancy,Neonatal;

Classifications:



External Ids:

ICD10 via Orphanet 34 Q77.8
Orphanet 59 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 HGMD
31 HMDB
32 HPO
33 ICD10
34 ICD10 via Orphanet
35 ICD9CM
36 IUPHAR
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44 MeSH
45 MESH via Orphanet
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54 NINDS
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58 OMIM via Orphanet
62 PubMed
64 QIAGEN
69 SNOMED-CT via HPO
70 TGDB
71 Tocris
72 UMLS
73 UMLS via Orphanet
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