raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01

ORPHA:695038

Small omphalocele

Synonyms: Minor omphalocele

Type: Clinical subtype
Group: Subtype of disorder
Inheritance: Not applicable
Status: active

Orphadata ships no English definition for this code.

1

Names in Orphadata languages

9 of 12 languages

Lang	Name	Synonyms
en	Small omphalocele	Minor omphalocele
fr	Petite omphalocèle	Omphalocèle mineure
de	Kleine Omphalozele	Omphalozele minor
es	Onfalocele pequeño	Onfalocele menor
it	Onfalocele piccolo	Onfalocele minore
nl	Kleine omfalocele
pt	Small omphalocele
pl	Small omphalocele	= en
cs	Small omphalocele	= en

2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Preferential parent (Orphanet linearisation):

ORPHA:93890Rare developmental defect during embryogenesis

Parents in the classifications (1):

ORPHA:660Omphalocele
rare developmental anomalies during embryogenesis; rare abdominal surgical diseases

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card

Orphanet page: orpha.net/en/disease/detail/695038
This record as JSON: /data/d/695038.json