Related Conditions
Global developmental delay(child)
Cognitive developmental delay(child)
Developmental delay in feeding(child)
Developmental delay in fine motor function(child)
Developmental delay in social skills(child)
Koolen De Vries syndrome(child)
Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome(child)
Cardiocranial syndrome Pfeiffer type(child)
Bohring Opitz syndrome(child)
Frank-Ter Haar syndrome(child)
Developmental delay, epilepsy, neonatal diabetes syndrome(child)
Obesity, colitis, hypothyroidism, cardiac hypertrophy, developmental delay syndrome(child)
Trigonocephaly, short stature, developmental delay syndrome(child)
CDKL5 deficiency disorder(child)
Spondyloepimetaphyseal dysplasia Geneviève type(child)
Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome(child)
Intellectual disability, craniofacial dysmorphism, cryptorchidism syndrome(child)
Congenital cataract, hearing loss, severe developmental delay syndrome(child)
Trilineage bone marrow failure with developmental delay syndrome(child)
Lethal polymalformative syndrome Boissel type(child)
Quick Facts
- SNOMED CT
- 248290002
- UMLS CUI
- C0424605
- Fully Specified Name
- Developmental delay (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.