microgastria-limb reduction defect syndrome
MONDO:0007993Mondo
Findings
No curated finding names microgastria-limb reduction defect syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
This syndrome is characterized by the association of microgastria with a limb reduction defect.
Definition from the Mondo Disease Ontology (MONDO:0007993), read 2026-09-29. CC BY 4.0.
Features
48 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Abnormal morphology of the radiusHPOHP:0002818
- Very frequent (80% to 99% of cases)
- Abnormality of the spleenHPOHP:0001743
- Very frequent (80% to 99% of cases)
- EsophagitisHPOHP:0100633
- Very frequent (80% to 99% of cases)
- Failure to thriveHPOHP:0001508
- Very frequent (80% to 99% of cases)
- Feeding difficultiesHPOHP:0011968
- Very frequent (80% to 99% of cases)
- Gastroesophageal refluxHPOHP:0002020
- Very frequent (80% to 99% of cases)
- Growth delayHPOHP:0001510
- Very frequent (80% to 99% of cases)
- Hiatus herniaHPOHP:0002036
- Very frequent (80% to 99% of cases)
- MicrogastriaHPOHP:0100841
- Very frequent (80% to 99% of cases)
- Short thumbHPOHP:0009778
- Very frequent (80% to 99% of cases)
- Abnormal finger morphologyHPOHP:0001167
- Frequent (30% to 79% of cases)
- Abnormal humerus morphologyHPOHP:0031095
- Frequent (30% to 79% of cases)
Show the remaining 36
- Abnormal metacarpal morphologyHPOHP:0005916
- Frequent (30% to 79% of cases)
- Congenital muscular torticollisHPOHP:0005988
- Frequent (30% to 79% of cases)
- Frontal bossingHPOHP:0002007
- Frequent (30% to 79% of cases)
- Multicystic kidney dysplasiaHPOHP:0000003
- Frequent (30% to 79% of cases)
- PlagiocephalyHPOHP:0001357
- Frequent (30% to 79% of cases)
- Prominent foreheadHPOHP:0011220
- Frequent (30% to 79% of cases)