MCID: HRN025
MIFTS: 5

Hernia, Double Inguinal

Aliases & Classifications for Hernia, Double Inguinal

MalaCards integrated aliases for Hernia, Double Inguinal:

Name: Hernia, Double Inguinal 56

Characteristics:

OMIM:

56
Inheritance:
autosomal dominant with sex influence


HPO:

31
hernia, double inguinal:
Inheritance autosomal dominant inheritance


External Ids:

OMIM 56 142350
MedGen 41 C0860251
SNOMED-CT via HPO 68 263681008 396232000

Summaries for Hernia, Double Inguinal

MalaCards based summary : Hernia, Double Inguinal Related phenotype is inguinal hernia.

More information from OMIM: 142350

Related Diseases for Hernia, Double Inguinal

Symptoms & Phenotypes for Hernia, Double Inguinal

Human phenotypes related to Hernia, Double Inguinal:

31
# Description HPO Frequency HPO Source Accession
1 inguinal hernia 31 HP:0000023

Symptoms via clinical synopsis from OMIM:

56
Abdomen:
bilateral inguinal hernia

Clinical features from OMIM:

142350

Drugs & Therapeutics for Hernia, Double Inguinal

Search Clinical Trials , NIH Clinical Center for Hernia, Double Inguinal

Genetic Tests for Hernia, Double Inguinal

Anatomical Context for Hernia, Double Inguinal

Publications for Hernia, Double Inguinal

Articles related to Hernia, Double Inguinal:

# Title Authors PMID Year
1
Congenital inheritance of inguinal hernia. 56
18137066 1949

Variations for Hernia, Double Inguinal

Expression for Hernia, Double Inguinal

Search GEO for disease gene expression data for Hernia, Double Inguinal.

Pathways for Hernia, Double Inguinal

GO Terms for Hernia, Double Inguinal

Sources for Hernia, Double Inguinal

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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