MCID: ZRS001
MIFTS: 5

Zori Stalker Williams Syndrome

Categories: Genetic diseases, Rare diseases

Aliases & Classifications for Zori Stalker Williams Syndrome

MalaCards integrated aliases for Zori Stalker Williams Syndrome:

Name: Zori Stalker Williams Syndrome 52 71
Familial Short Stature, Developmental Delay, Pectus Abnormalities, Distinctive Facies, and Dysplastic Nails 52
Pectus Excavatum, Macrocephaly and Dysplastic Nails 52

Classifications:



External Ids:

UMLS 71 C2931302

Summaries for Zori Stalker Williams Syndrome

MalaCards based summary : Zori Stalker Williams Syndrome, also known as familial short stature, developmental delay, pectus abnormalities, distinctive facies, and dysplastic nails, is related to pectus excavatum, macrocephaly, short stature, and dysplastic nails.

Related Diseases for Zori Stalker Williams Syndrome

Diseases related to Zori Stalker Williams Syndrome via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 pectus excavatum, macrocephaly, short stature, and dysplastic nails 12.4

Symptoms & Phenotypes for Zori Stalker Williams Syndrome

Drugs & Therapeutics for Zori Stalker Williams Syndrome

Search Clinical Trials , NIH Clinical Center for Zori Stalker Williams Syndrome

Genetic Tests for Zori Stalker Williams Syndrome

Anatomical Context for Zori Stalker Williams Syndrome

Publications for Zori Stalker Williams Syndrome

Variations for Zori Stalker Williams Syndrome

Expression for Zori Stalker Williams Syndrome

Search GEO for disease gene expression data for Zori Stalker Williams Syndrome.

Pathways for Zori Stalker Williams Syndrome

GO Terms for Zori Stalker Williams Syndrome

Sources for Zori Stalker Williams Syndrome

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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