Acrorenal syndrome

disorder

SNOMED 720458005CUI C3495490

Overview

Acrorenal 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.

Kidney malformation

Very frequent (80-99%)HP:0012210

Renal hypoplasia/aplasia

Very frequent (80-99%)HP:0008678

Split hand

Very frequent (80-99%)HP:0001171

Abnormal morphology of ulna

Frequent (30-79%)HP:0040071

Abnormal tibia morphology

Frequent (30-79%)HP:0002992

Absent/underdeveloped radius

Frequent (30-79%)HP:0006501

Renal insufficiency

Frequent (30-79%)HP:0000083

Abnormal eye

Occasional (5-29%)HP:0000478

Abnormality of vision

Occasional (5-29%)HP:0000504

Cleft of palate

Occasional (5-29%)HP:0000175

Decreased projection of lower jaw

Occasional (5-29%)HP:0000347

Absent fingers

HP:0009380

Related Conditions

Multiple malformation syndrome with limb defect as major feature(parent)

Congenital anomaly of the kidney(parent)

Congenital anomaly of limb(parent)

Hereditary nephropathy(parent)

Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT: 720458005
UMLS CUI: C3495490
Fully Specified Name: Acrorenal syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 12

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.