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Congenital penoscrotal transposition

disorder
SNOMED 312005008CUI C1868854

Overview

Congenital penoscrotal transposition 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.

Abnormal external genitalia morphology
Very frequent (80-99%)HP:0000811
Abnormality of the reproductive system
Very frequent (80-99%)HP:0000078
Abnormality of the ureter
Very frequent (80-99%)HP:0000069
Bilateral single transverse palmar creases
Very frequent (80-99%)HP:0007598
Cerebral cortex atrophy
Very frequent (80-99%)HP:0002120
Curvature of little finger
Very frequent (80-99%)HP:0004209
Decreased projection of mandible
Very frequent (80-99%)HP:0000347
Disease of the heart muscle
Very frequent (80-99%)HP:0001638
Hypospadias
Very frequent (80-99%)HP:0000047
Pectus carinatum
Very frequent (80-99%)HP:0000768
Prepenile scrotum
Very frequent (80-99%)HP:0100600
Renal adysplasia
Very frequent (80-99%)HP:0000110
Renal aplasia
Very frequent (80-99%)HP:0000104
Urethra issue
Very frequent (80-99%)HP:0000795
Wide-spaced nipples
Very frequent (80-99%)HP:0006610
Indentation of chin
Frequent (30-79%)HP:0010751
Palpebronasal fold
Frequent (30-79%)HP:0000286
Prominent back of the head
Frequent (30-79%)HP:0000269
Shawl scrotum
Frequent (30-79%)HP:0000049
Patellar aplasia
Occasional (5-29%)HP:0006443

Quick Facts

SNOMED CT
312005008
UMLS CUI
C1868854
Fully Specified Name
Congenital penoscrotal transposition (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
20
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.