Overview
Mosaic trisomy chromosome 7 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.
Depigmentation/hyperpigmentation of skin
Frequent (30-79%)HP:0007483
Growth delay as children
Frequent (30-79%)HP:0008897
Intrauterine growth retardation, IUGR
Frequent (30-79%)HP:0001511
Macular hypopigmentation
Frequent (30-79%)HP:0007988
Birth weight less than 10th percentile
Occasional (5-29%)HP:0001518
Cardiac anomaly
Occasional (5-29%)HP:0001627
Cleft of palate
Occasional (5-29%)HP:0000175
Decreased projection of mandible
Occasional (5-29%)HP:0000347
Enamel dysplasia
Occasional (5-29%)HP:0006297
Fetal cystic hygroma
Occasional (5-29%)HP:0010878
Global developmental delay, mild
Occasional (5-29%)HP:0011342
High blood pressure
Occasional (5-29%)HP:0000822
Hypertrichosis
Occasional (5-29%)HP:0000998
Inguinal hernia
Occasional (5-29%)HP:0000023
Large head
Occasional (5-29%)HP:0000256
Premature birth
Occasional (5-29%)HP:0001622
Renal adysplasia
Occasional (5-29%)HP:0000110
Unbalanced face
Occasional (5-29%)HP:0000324
Related Conditions
Quick Facts
- SNOMED CT
- 764630003
- UMLS CUI
- C2931631
- Fully Specified Name
- Mosaic trisomy 7 syndrome (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.