axial mesodermal dysplasia spectrum
Findings
No curated finding names axial mesodermal dysplasia spectrum yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Axial mesodermal dysplasia spectrum is a rare developmental defect during embryogenesis syndrome characterized by congenital manifestations of both oculo-auriculo-vertebral spectrum and caudal regression sequence. Phenotype is highly variable but patients typically present facial dysmorphism (incl. asymmetry, hypertelorism), auricular abnormalities (e.g. preauricular tags, microtia, absence of middle ear ossicles), skeletal malformations (hemivertebrae, hip dislocation, sacral agenesis/dysplasia, talipes equinovarus, flexion deformity of lower limbs), cardiac defects (dextrocardia, septal defects), renal and genitourinary anomalies (such as renal agensis/dysplasia, abnormal external genitalia, cryptorchidia), as well as anal anomalies such as anal atresia and rectovesical fistula.
Definition from the Mondo Disease Ontology (MONDO:0015944), read 2026-09-29. CC BY 4.0.
Features
42 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 gastrointestinal tract morphologyHPOHP:0012718
- Very frequent (80% to 99% of cases)
- Abnormal intestine morphologyHPOHP:0002242
- Very frequent (80% to 99% of cases)
- Abnormal morphology of female internal genitaliaHPOHP:0000008
- Very frequent (80% to 99% of cases)
- Abnormal pelvic girdle bone morphologyHPOHP:0002644
- Very frequent (80% to 99% of cases)
- Abnormal rib morphologyHPOHP:0000772
- Very frequent (80% to 99% of cases)
- Abnormal vertebral body morphologyHPOHP:0003312
- Very frequent (80% to 99% of cases)
Show the remaining 30
- Abnormality of the urinary systemHPOHP:0000079
- Very frequent (80% to 99% of cases)
- Anal atresiaHPOHP:0002023
- Very frequent (80% to 99% of cases)
- Anorectal anomalyHPOHP:0012732
- Very frequent (80% to 99% of cases)
- Aplasia/Hypoplasia of the lungsHPOHP:0006703
- Very frequent (80% to 99% of cases)
- Cerebral cortical atrophyHPOHP:0002120
- Very frequent (80% to 99% of cases)
- Congenital diaphragmatic herniaHPOHP:0000776
Where it sits
Other names
2 names
Resolves to: axial mesodermal dysplasia spectrum
- Also called
- blastogenesis defectRussell-Weaver-Bull syndrome