Aliases & Classifications for Purpura Simplex

MalaCards integrated aliases for Purpura Simplex:

Name: Purpura Simplex 56 52 71

Characteristics:

OMIM:

56
Inheritance:
autosomal dominant


HPO:

31
purpura simplex:
Inheritance autosomal dominant inheritance


Classifications:



Summaries for Purpura Simplex

MalaCards based summary : Purpura Simplex is related to purpura and ptosis. Affiliated tissues include testes and placenta, and related phenotypes are ptosis and purpura

More information from OMIM: 179000

Related Diseases for Purpura Simplex

Diseases related to Purpura Simplex via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 purpura 10.3
2 ptosis 9.8
3 vasculitis 9.8

Symptoms & Phenotypes for Purpura Simplex

Human phenotypes related to Purpura Simplex:

31
# Description HPO Frequency HPO Source Accession
1 ptosis 31 HP:0000508
2 purpura 31 HP:0000979
3 epistaxis 31 HP:0000421
4 bruising susceptibility 31 HP:0000978
5 menorrhagia 31 HP:0000132

Symptoms via clinical synopsis from OMIM:

56
Eyes:
ptosis

G U:
menorrhagia

Lab:
positive tourniquet test
clotting tests normal

Nose:
epistaxis

Skin:
purpura of extremities
ecchymoses on slight trauma

Clinical features from OMIM:

179000

Drugs & Therapeutics for Purpura Simplex

Search Clinical Trials , NIH Clinical Center for Purpura Simplex

Genetic Tests for Purpura Simplex

Anatomical Context for Purpura Simplex

MalaCards organs/tissues related to Purpura Simplex:

40
Testes, Placenta

Publications for Purpura Simplex

Articles related to Purpura Simplex:

(show all 17)
# Title Authors PMID Year
1
Combined inheritance of purpura simplex and ptosis in four generations of one family. 56 61
13208770 1954
2
Experience of a year of adult hospital dermatology consultations. 61
25384904 2015
3
[Correlation between HLA-DQA1 allele and anaphylactoid purpura in juvenile Hans residing in Inner Mongolia]. 61
11836690 2002
4
[Purpura simplex]. 61
9833530 1998
5
Capillaritis (purpura simplex) associated with use of aminoglutethimide in Cushing's syndrome. 61
7847422 1994
6
Drug-induced purpura simplex: clinical and histological characteristics. 61
8129346 1993
7
Spontaneous Bruising in a Family Practice Population: How common and how benign is it? 61
21221312 1992
8
Purpura simplex (inflammatory purpura without vasculitis): a clinicopathologic study of 174 cases. 61
1791222 1991
9
Early histopathology of the cutaneous capillary fragility test (Rumpel-Leede). 61
438390 1979
10
[Immunopathological study of Gougerot-Ruiter's vasculitis (author's transl)]. 61
326131 1977
11
[Davis' disease (purpura simplex hereditaria familiaris)]. 61
5761056 1968
12
[Syndrome of allergic vascular purpura. (Purpura rheumatica, purpura simplex, peliosis rheumatica, capillarotoxicosis, purpura anaphylactoides, purpura allergica, purpura Schönlein-Henoch]. 61
5658826 1968
13
[Grave transitory hemorrhagic diathesis in pregnancy; thrombokinase intoxication caused by premature detachment of the placenta in familial purpura simplex]. 61
13572460 1958
14
[Purpura simplex hemosiderotica]. 61
13465860 1957
15
Familial hereditary purpura simplex with Schönlein-Henoch syndrome; response to corticotropin (ACTH), cortisone, and antihistaminics. 61
13242408 1955
16
Purpura simplex due to antihistaminic drugs. 61
14907267 1951
17
Purpura simplex. 61
21065808 1946

Variations for Purpura Simplex

Expression for Purpura Simplex

Search GEO for disease gene expression data for Purpura Simplex.

Pathways for Purpura Simplex

GO Terms for Purpura Simplex

Sources for Purpura Simplex

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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