Overview
Acrorenal mandibular 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.
Foot ectrodactyly
Very frequent (80-99%)HP:0001839
Renal hypoplasia/aplasia
Very frequent (80-99%)HP:0008678
Rudimentary to absent tibiae
Very frequent (80-99%)HP:0006426
Shortening of radius
Very frequent (80-99%)HP:0002984
Small to absent fibula
Very frequent (80-99%)HP:0006381
Split hand
Very frequent (80-99%)HP:0001171
Abnormal clavicles
Frequent (30-79%)HP:0000889
Abnormality of the sense of smell
Frequent (30-79%)HP:0004408
Decreased amniotic fluid index
Frequent (30-79%)HP:0001562
Dislocated femoral heads
Frequent (30-79%)HP:0002827
Double uterus
Frequent (30-79%)HP:0003762
Heart shaped uterus
Frequent (30-79%)HP:0000813
High arched palate
Frequent (30-79%)HP:0000218
Hypoplastic mandible
Frequent (30-79%)HP:0000347
Intrauterine growth retardation, IUGR
Frequent (30-79%)HP:0001511
Pectus carinatum
Frequent (30-79%)HP:0000768
Poorly developed lungs
Frequent (30-79%)HP:0002089
Posteriorly angulated ears
Frequent (30-79%)HP:0000358
Short neck
Frequent (30-79%)HP:0000470
Slender ribs
Frequent (30-79%)HP:0000883
Small malar bone
Frequent (30-79%)HP:0010669
Abnormal connection between trachea and esophagus
Occasional (5-29%)HP:0002575
Aplasia/Hypoplasia of the tongue
Occasional (5-29%)HP:0010295
Cleft lip, cleft palate
Occasional (5-29%)HP:0000202
Decreased height of philtrum
Occasional (5-29%)HP:0000322
Decreased transverse dimension of face
Occasional (5-29%)HP:0000275
Diaphragmatic hernia
Occasional (5-29%)HP:0000776
Down-slanting palpebral fissure
Occasional (5-29%)HP:0000494
Hemivertebra
Occasional (5-29%)HP:0002937
Hunched back
Occasional (5-29%)HP:0002808
Related Conditions
Multiple malformation syndrome with facial-limb defects as major feature(parent)
Congenital anomaly of the kidney(parent)
Longitudinal deficiency of limb(parent)
Recessive hereditary disorder (autosomal)(parent)
Congenital anomaly of mandible(parent)
Hereditary disorder of musculoskeletal system(parent)
Hereditary nephropathy(parent)
Developmental hereditary disorder(parent)
Quick Facts
- SNOMED CT
- 720414005
- UMLS CUI
- C1860166
- Fully Specified Name
- Acrorenal mandibular syndrome (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.