Overview
Holzgreve Wagner Rehder syndrome 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.
Abnormality of cardiovascular system morphology
Very frequent (80-99%)HP:0030680
Absent/small lungs
Very frequent (80-99%)HP:0006703
Cleft of palate
Very frequent (80-99%)HP:0000175
Decreased amniotic fluid index
Very frequent (80-99%)HP:0001562
Intrauterine growth retardation, IUGR
Very frequent (80-99%)HP:0001511
Polydactyly of the hand
Very frequent (80-99%)HP:0001161
Renal hypoplasia/aplasia
Very frequent (80-99%)HP:0008678
2 vessel cord
Frequent (30-79%)HP:0001195
Abnormal metacarpal morphology
Frequent (30-79%)HP:0005916
Abnormal morphology of ulna
Frequent (30-79%)HP:0040071
Abnormality of the mesentery
Frequent (30-79%)HP:0100016
Abnormally ossified vertebrae
Frequent (30-79%)HP:0100569
Aplasia/Hypoplasia of the tongue
Frequent (30-79%)HP:0010295
Bilobed tongue
Frequent (30-79%)HP:0010297
Hypoplastic or absent corpus callosum
Frequent (30-79%)HP:0007370
Large ears
Frequent (30-79%)HP:0000400
Posteriorly angulated ears
Frequent (30-79%)HP:0000358
Pterygium colli
Frequent (30-79%)HP:0000465
Rib anomalies
Frequent (30-79%)HP:0000772
Stiff joint
Frequent (30-79%)HP:0001387
Tall shaped head
Frequent (30-79%)HP:0000262
Cleft of upper lip
HP:0000204
Hypoplastic left heart
HP:0004383
Renal aplasia
HP:0000104
Small kidneys
HP:0000089
Related Conditions
Digestive system hereditary disorder(parent)
Cleft palate with cleft lip(parent)
Recessive hereditary disorder (autosomal)(parent)
Renal agenesis(parent)
Hereditary nephropathy(parent)
Potter's facies(parent)
Hereditary disorder of musculoskeletal system(parent)
Multiple system malformation syndrome(parent)
Congenital anomaly of face bones(parent)
Developmental hereditary disorder(parent)
Quick Facts
- SNOMED CT
- 783159001
- UMLS CUI
- C1856095
- Fully Specified Name
- Holzgreve syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 25
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.