Overview
X-linked intellectual disability Pai type is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Mental and motor retardation
Very frequent (80-99%)HP:0001263
Mental retardation, severe
Very frequent (80-99%)HP:0010864
respiratory infections, recurrent
Very frequent (80-99%)HP:0002205
Seizures
Very frequent (80-99%)HP:0001250
Intrauterine growth retardation, IUGR
Frequent (30-79%)HP:0001511
Speech difficulties
Frequent (30-79%)HP:0000750
Convex bridge of nose
Occasional (5-29%)HP:0000426
Cryptorchidism
Occasional (5-29%)HP:0000028
Gait disturbance
Occasional (5-29%)HP:0001288
Hydrocele testis
Occasional (5-29%)HP:0000034
Hypertonia
Occasional (5-29%)HP:0001276
Inguinal hernia
Occasional (5-29%)HP:0000023
Narrow mouth
Occasional (5-29%)HP:0000160
Palpebronasal fold
Occasional (5-29%)HP:0000286
Prominent ear
Occasional (5-29%)HP:0000411
Retarded ossification
Occasional (5-29%)HP:0002750
Spastic quadriplegia
Occasional (5-29%)HP:0002510
Tapering fingers
Occasional (5-29%)HP:0001182
Quick Facts
- SNOMED CT
- 719011002
- UMLS CUI
- C4305026
- Fully Specified Name
- X-linked intellectual disability Pai type (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 18
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.