Overview
Renal hepatic pancreatic dysplasia 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.
Dysplastic kidneys
Very frequent (80-99%)HP:0000110
Enlarged liver
Very frequent (80-99%)HP:0002240
Abnormal liver parenchyma morphology
Frequent (30-79%)HP:0030146
Abnormal pancreatic duct morphology
Frequent (30-79%)HP:0030992
Alanine aminotransferase increased
Frequent (30-79%)HP:0031964
Decreased amniotic fluid index
Frequent (30-79%)HP:0001562
Elevated gamma-glutamyltransferase level
Frequent (30-79%)HP:0030948
Elevated serum aspartate aminotransferase
Frequent (30-79%)HP:0031956
Enlarged kidney
Frequent (30-79%)HP:0000105
High blood bilirubin levels
Frequent (30-79%)HP:0002904
Neonatal cholestatic liver disease
Frequent (30-79%)HP:0006566
Pancreatic dysplasia
Frequent (30-79%)HP:0005232
Pancreatic fibrosis
Frequent (30-79%)HP:0100732
Renal cyst
Frequent (30-79%)HP:0000107
Renal failure in adulthood
Frequent (30-79%)HP:0000083
Respiratory distress, neonatal
Frequent (30-79%)HP:0002643
Type I diabetes mellitus
Frequent (30-79%)HP:0100651
Abnormal vertebral bodies
Occasional (5-29%)HP:0003312
Absent spleen
Occasional (5-29%)HP:0001746
Aortic stenosis
Occasional (5-29%)HP:0001650
Cirrhosis
Occasional (5-29%)HP:0001394
Increased circulating amylase level
Occasional (5-29%)HP:0410288
Increased circulating lipoprotein lipase concentration
Occasional (5-29%)HP:0033478
increased pulmonary artery pressure
Occasional (5-29%)HP:0004890
Large spleen
Occasional (5-29%)HP:0001744
Liver cysts
Occasional (5-29%)HP:0001407
Liver fibrosis
Occasional (5-29%)HP:0001395
Multiple pancreatic cysts
Occasional (5-29%)HP:0001737
Nonimmune hydrops fetalis
Occasional (5-29%)HP:0001790
PDA
Occasional (5-29%)HP:0001643
Related Conditions
Fibrosis of pancreas(parent)
Multiple system malformation syndrome(parent)
Congenital cystic kidney disease(parent)
Recessive hereditary disorder (autosomal)(parent)
Congenital anomaly of liver(parent)
Digestive system hereditary disorder(parent)
Hereditary nephropathy(parent)
Congenital malformation of pancreas(parent)
Congenital anomaly of the kidney(parent)
Hereditary disorder of endocrine system(parent)
Developmental hereditary disorder(parent)
Quick Facts
- SNOMED CT
- 763891005
- UMLS CUI
- C2673883
- Fully Specified Name
- Renal hepatic pancreatic dysplasia (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 30
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.