Rare diseases · Sign or symptom
Hernia
HP:0100790
In everyday care
Most people with this sign do not have a rare disease — it appears in common conditions far more often. These general reference pages cover the same topic:
Rare diseases that can present with this54
Very common80–99%
8Common30–79%
22- 6p22microdeletion syndrome
- Arthrochalasia Ehlers-Danlos syndrome
- Autosomal dominant cutis laxa
- Autosomal dominant spastic paraplegia type 29
- Autosomal recessive cutis laxa type 1
- Cerebrofaciothoracic dysplasia
- Classical Ehlers-Danlos syndrome
- Congenital limbs-face contractures-hypotonia-developmental delay syndrome
- Distal deletion 9p syndrome
- Distal duplication 5q syndrome
- Fetal hydantoin syndrome
- Focal dermal hypoplasia
- Hereditary hyperekplexia
- Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency
- Mosaic trisomy 2 syndrome
- Mucopolysaccharidosis type 4
- Mucopolysaccharidosis type 6
- Non-distal duplication 13q syndrome
- Pancreatic hypoplasia-diabetes-congenital heart disease syndrome
- Sialidosis type 1
- Trisomy 13 syndrome
- Trisomy 18 syndrome
The range is how often this sign appears among people diagnosed with each disease — it is not a probability of having any of them. Many of these signs also occur in common, non-rare conditions. A sign on this page is a conversation to have with a clinician, not a conclusion.
Part of the broader category
Also called: Hernias
Tracking symptoms like this for someone? Eleplan keeps symptoms, diagnoses, medications and every specialist in one plan.
Start free with EleplanThis page uses the Human Phenotype Ontology (2026-06-23) — Human Phenotype Ontology Consortium, hpo.jax.org. Disease associations from Orphanet (INSERM), CC BY 4.0. Content is educational and is not medical advice.