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Renal agenesis

disorder
SNOMED 204942005CUI C0542519

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Renal aplasia
Always present (100%)HP:0000104
Unilateral renal agenesis
Frequent (30-79%)HP:0000122
Ureteral agenesis
Frequent (30-79%)HP:0012300
Absent anus
Occasional (5-29%)HP:0002023
Absent ductus deferens
Occasional (5-29%)HP:0012873
Absent/small bladder
Occasional (5-29%)HP:0010476
Absent/underdeveloped uterus
Occasional (5-29%)HP:0008684
Bilateral renal agenesis
Occasional (5-29%)HP:0010958
Decreased amniotic fluid index
Occasional (5-29%)HP:0001562
Fetal foot inversion
Occasional (5-29%)HP:0001762
High blood pressure
Occasional (5-29%)HP:0000822
Poorly developed lungs
Occasional (5-29%)HP:0002089
Potter facies
Occasional (5-29%)HP:0002009
Proteinuria
Occasional (5-29%)HP:0000093
Renal insufficiency
Occasional (5-29%)HP:0000083
VSD
Occasional (5-29%)HP:0001629

Quick Facts

SNOMED CT
204942005
UMLS CUI
C0542519
Fully Specified Name
Renal agenesis (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
16
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.