congenital muscular dystrophy with intellectual disability
MONDO:0018278Mondo
Findings
No curated finding names congenital muscular dystrophy with intellectual disability yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Features
43 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.
- Elevated circulating creatine kinase activityHPOHP:0003236
- Very frequent (80% to 99% of cases)
- Floppy infantHPOHP:0008947
- Very frequent (80% to 99% of cases)
- Hypoglycosylation of alpha-dystroglycanHPOHP:0030046
- Very frequent (80% to 99% of cases)
- Intellectual disabilityHPOHP:0001249
- Very frequent (80% to 99% of cases)
- Reduced muscle fiber alpha dystroglycanHPOHP:0030099
- Very frequent (80% to 99% of cases)
- Calf muscle hypertrophyHPOHP:0008981
- Frequent (30% to 79% of cases)
- Cerebral cortical atrophyHPOHP:0002120
- Frequent (30% to 79% of cases)
- Fatigable weakness of skeletal musclesHPOHP:0030197
- Frequent (30% to 79% of cases)
- Feeding difficultiesHPOHP:0011968
- Frequent (30% to 79% of cases)
- Global developmental delayHPOHP:0001263
- Frequent (30% to 79% of cases)
- Limb-girdle muscle weaknessHPOHP:0003325
- Frequent (30% to 79% of cases)
- MicrocephalyHPOHP:0000252
- Frequent (30% to 79% of cases)
Show the remaining 31
- Motor delayHPOHP:0001270
- Frequent (30% to 79% of cases)
- Multiple joint contracturesHPOHP:0002828
- Frequent (30% to 79% of cases)
- Poor gross motor coordinationHPOHP:0007015
- Frequent (30% to 79% of cases)
- Abnormal periventricular white matter morphologyHPOHP:0002518
- Occasional (5% to 29% of cases)
- Abnormal pons morphologyHPOHP:0007361
- Occasional (5% to 29% of cases)
- Abnormality of connective tissueHPOHP:0003549
- Occasional (5% to 29% of cases)
Genes
5 genes
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.
- FKRPHGNC:17997
- Supportive · Orphanet · Autosomal recessive · 2021
- GMPPBHGNC:22932
- Supportive · Orphanet · Autosomal recessive · 2021
- LARGE1HGNC:6511
- Supportive · Orphanet · Autosomal recessive · 2021
- POMT1HGNC:9202
- Supportive · Orphanet · Autosomal recessive · 2021
- POMT2HGNC:19743
- Supportive · Orphanet · Autosomal recessive · 2021
Where it sits
Other names
2 names
Resolves to: congenital muscular dystrophy with intellectual disability
- Also called
- CMD with intellectual disabilityCMD-MR