microcephaly-glomerulonephritis-marfanoid habitus syndrome
MONDO:0009565Mondo
Findings
No curated finding names microcephaly-glomerulonephritis-marfanoid habitus syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
This syndrome is characterized by intellectual deficit, marfanoid habitus, microcephaly, and glomerulonephritis.
Definition from the Mondo Disease Ontology (MONDO:0009565), read 2026-09-29. CC BY 4.0.
Features
11 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.
- ArachnodactylyHPOHP:0001166
- Frequent (30% to 79% of cases)
- Chronic kidney diseaseHPOHP:0012622
- Frequent (30% to 79% of cases)
- Disproportionate tall statureHPOHP:0001519
- Frequent (30% to 79% of cases)
- GlomerulonephritisHPOHP:0000099
- Frequent (30% to 79% of cases)
- High palateHPOHP:0000218
- Frequent (30% to 79% of cases)
- Joint hypermobilityHPOHP:0001382
- Frequent (30% to 79% of cases)
- Mandibular prognathiaHPOHP:0000303
- Frequent (30% to 79% of cases)
- Moderate intellectual disabilityHPOHP:0002342
- Frequent (30% to 79% of cases)
- Primary microcephalyHPOHP:0011451
- Frequent (30% to 79% of cases)
- Thoracic kyphosisHPOHP:0002942
- Frequent (30% to 79% of cases)
- VentriculomegalyHPOHP:0002119
- Frequent (30% to 79% of cases)