rapadilino syndrome
Findings
No curated finding names rapadilino syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
RAPADILINO syndrome is a syndrome for which the acronym indicates the principal signs: RA for radial ray defect, PA for both patellae hypoplasia or aplasia and cleft or highly arched palate, DI for diarrhea and dislocated joints, LI for little size and limb malformations, NO for long, slender nose and normal intelligence.
Definition from the Mondo Disease Ontology (MONDO:0009955), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal recessive inheritance
HPO, annotations 2026-09-02
Features
21 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.
- Aplasia/Hypoplasia of the radiusHPOHP:0006501
- 14 of 14 reported patients
- Frequent (30% to 79% of cases)
- Short statureHPOHP:0004322
- 13 of 14 reported patients
- Aplasia/Hypoplasia of the patellaHPOHP:0006498
- 12 of 14 reported patients
- Frequent (30% to 79% of cases)
- Feeding difficultiesHPOHP:0011968
- 12 of 14 reported patients
- Frequent (30% to 79% of cases)
- Intrauterine growth retardationHPOHP:0001511
- Very frequent (80% to 99% of cases)
- Postnatal growth retardationHPOHP:0008897
- Very frequent (80% to 99% of cases)
Show the remaining 9
- Joint dislocationHPOHP:0001373
- 8 of 14 reported patients
- Decreased circulating immunoglobulin concentrationHPOHP:0004313
- Occasional (5% to 29% of cases)
- Decreased total T cell countHPOHP:0005403
- Occasional (5% to 29% of cases)
- Mild intellectual disabilityHPOHP:0001256
- 2 of 14 reported patients
- PoikilodermaHPOHP:0001029
- 0 of 14 reported patients
- Sparse eyebrowHPOHP:0045075
- 0 of 13 reported patients
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- RECQL4HGNC:9949
- Strong · Genomics England PanelApp · Autosomal recessive · 2021
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Supportive · Orphanet · Autosomal recessive · 2021