Aliases & Classifications for Woronets Trait

MalaCards integrated aliases for Woronets Trait:

Name: Woronets Trait 58

Characteristics:

OMIM:

58
Inheritance:
autosomal dominant


HPO:

33
woronets trait:
Inheritance autosomal dominant inheritance


External Ids:

OMIM 58 194320
MedGen 43 C1860237
SNOMED-CT via HPO 70 263681008

Summaries for Woronets Trait

MalaCards based summary : Woronets Trait Related phenotype is red blood cell keratocytosis.

Description from OMIM: 194320

Related Diseases for Woronets Trait

Symptoms & Phenotypes for Woronets Trait

Human phenotypes related to Woronets Trait:

33
# Description HPO Frequency HPO Source Accession
1 red blood cell keratocytosis 33 HP:0005540

Symptoms via clinical synopsis from OMIM:

58
Heme:
distorted red blood cells resembling keratocytes
normal red cell life span

Clinical features from OMIM:

194320

Drugs & Therapeutics for Woronets Trait

Search Clinical Trials , NIH Clinical Center for Woronets Trait

Genetic Tests for Woronets Trait

Anatomical Context for Woronets Trait

Publications for Woronets Trait

Articles related to Woronets Trait:

# Title Authors Year
1
The Woronets trait: a new familial erythrocyte anomaly. ( 7378595 )
1980

Variations for Woronets Trait

Expression for Woronets Trait

Search GEO for disease gene expression data for Woronets Trait.

Pathways for Woronets Trait

GO Terms for Woronets Trait

Sources for Woronets Trait

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
20 FMA
29 GO
30 GTR
31 HGMD
32 HMDB
33 HPO
34 ICD10
35 ICD10 via Orphanet
36 ICD9CM
37 IUPHAR
38 KEGG
39 LifeMap
41 LOVD
43 MedGen
45 MeSH
46 MESH via Orphanet
47 MGI
50 NCI
51 NCIt
52 NDF-RT
55 NINDS
56 Novoseek
58 OMIM
59 OMIM via Orphanet
63 PubMed
65 QIAGEN
70 SNOMED-CT via HPO
71 SNOMED-CT via Orphanet
72 TGDB
73 Tocris
74 UMLS
75 UMLS via Orphanet
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