MCID: PFF006
MIFTS: 4

Pfeiffer Tietze Welte Syndrome

Categories: Rare diseases

Aliases & Classifications for Pfeiffer Tietze Welte Syndrome

MalaCards integrated aliases for Pfeiffer Tietze Welte Syndrome:

Name: Pfeiffer Tietze Welte Syndrome 52 71
Sagittal Craniostenosis, Bilateral Coloboma of the Iris, Craniofacial Dysmorphy, Asymmetrical Split Hand Malformation, Bilateral Syndactyly of 2nd-4th 52

Classifications:



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UMLS 71 C2931657

Summaries for Pfeiffer Tietze Welte Syndrome

MalaCards based summary : Pfeiffer Tietze Welte Syndrome, is also known as sagittal craniostenosis, bilateral coloboma of the iris, craniofacial dysmorphy, asymmetrical split hand malformation, bilateral syndactyly of 2nd-4th.

Related Diseases for Pfeiffer Tietze Welte Syndrome

Symptoms & Phenotypes for Pfeiffer Tietze Welte Syndrome

Drugs & Therapeutics for Pfeiffer Tietze Welte Syndrome

Search Clinical Trials , NIH Clinical Center for Pfeiffer Tietze Welte Syndrome

Genetic Tests for Pfeiffer Tietze Welte Syndrome

Anatomical Context for Pfeiffer Tietze Welte Syndrome

Publications for Pfeiffer Tietze Welte Syndrome

Articles related to Pfeiffer Tietze Welte Syndrome:

# Title Authors PMID Year
1
An unusual, possibly "new" MA/MR syndrome with sagittal craniosynostosis. 61
3034618 1987

Variations for Pfeiffer Tietze Welte Syndrome

Expression for Pfeiffer Tietze Welte Syndrome

Search GEO for disease gene expression data for Pfeiffer Tietze Welte Syndrome.

Pathways for Pfeiffer Tietze Welte Syndrome

GO Terms for Pfeiffer Tietze Welte Syndrome

Sources for Pfeiffer Tietze Welte 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
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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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