Rare diseases · Sign or symptom
Gastrointestinal hemorrhage
Gastrointestinal bleeding
HP:0002239
What it means
Hemorrhage affecting the gastrointestinal tract.
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 this91
Very common80–99%
9- Carney triad
- Congenital factor VII deficiency
- Familial dysfibrinogenemia
- Familial hypofibrinogenemia
- Hyperimmunoglobulinemia D with periodic fever
- Juvenile polyposis of infancy
- Lynch syndrome
- Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome
- Palmoplantar keratoderma-esophageal carcinoma syndrome
Common30–79%
12- Behçet disease
- Bernard-Soulier syndrome
- Capillary-lymphatic-venous malformation with segmental distribution
- Carney-Stratakis syndrome
- Congenital bile acid synthesis defect type 1
- Ebola hemorrhagic fever
- Familial colorectal cancer Type X
- Gastrointestinal stromal tumor
- Malignant atrophic papulosis
- Microscopic polyangiitis
- MPI-CDG
- Peutz-Jeghers 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: Gastrointestinal haemorrhage · GI haemorrhage · GI hemorrhage
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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.