short stature-brachydactyly-obesity-global developmental delay syndrome
MONDO:0014944Mondo
Findings
No curated finding names short stature-brachydactyly-obesity-global developmental delay syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
- Onset and course
- Congenital onset
HPO, annotations 2026-09-02
Features
85 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.
- Atonic seizureHPOHP:0010819
- 1 of 1 reported patient
- BrachycephalyHPOHP:0000248
- 1 of 1 reported patient
- Deeply set eyeHPOHP:0000490
- 1 of 1 reported patient
- Very frequent (80% to 99% of cases)
- Delayed ability to walkHPOHP:0031936
- 6 of 6 reported patients
- Delayed CNS myelinationHPOHP:0002188
- 1 of 1 reported patient
- Delayed speech and language developmentHPOHP:0000750
- 4 of 4 reported patients
- Failure to thriveHPOHP:0001508
- 1 of 1 reported patient
- Feeding difficultiesHPOHP:0011968
- 1 of 1 reported patient
- Occasional (5% to 29% of cases)
- Frontal hirsutismHPOHP:0011335
- 1 of 1 reported patient
- Gastroesophageal refluxHPOHP:0002020
- 1 of 1 reported patient
- Global developmental delayHPOHP:0001263
- 6 of 6 reported patients
- Very frequent (80% to 99% of cases)
- Intrauterine growth retardationHPOHP:0001511
- 1 of 1 reported patient
Show the remaining 73
- LaryngomalaciaHPOHP:0001601
- 1 of 1 reported patient
- Occasional (5% to 29% of cases)
- Long philtrumHPOHP:0000343
- 1 of 1 reported patient
- Very frequent (80% to 99% of cases)
- PolyhydramniosHPOHP:0001561
- 1 of 1 reported patient
- PtosisHPOHP:0000508
- 1 of 1 reported patient
- Rectal prolapseHPOHP:0002035
- 1 of 1 reported patient
- Recurrent urinary tract infectionsHPOHP:0000010
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.
- PRMT7HGNC:25557
- Definitive · G2P · Autosomal recessive · 2015
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2022
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Supportive · Orphanet · Autosomal recessive · 2021
Where it sits
Other names
2 names
Resolves to: short stature-brachydactyly-obesity-global developmental delay syndrome
- Also called
- SBIDDSshort stature, brachydactyly, intellectual developmental disability, and seizures