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Devriendt Vandenberghe Fryns syndrome

disorder
SNOMED 720981000CUI C4303740

Overview

Devriendt Vandenberghe Fryns 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.

Mental retardation, mild
Very frequent (80-99%)HP:0001256
Primary hypogonadism
Very frequent (80-99%)HP:0000815
Total alopecia
Very frequent (80-99%)HP:0007418

Related Conditions

Hereditary disorder of endocrine system(parent)
Hereditary disorder of the integument(parent)
Reproductive system hereditary disorder(parent)
Primary hypogonadism(parent)
Congenital alopecia(parent)
Developmental hereditary disorder(parent)
Genetic intellectual disability(parent)

Quick Facts

SNOMED CT
720981000
UMLS CUI
C4303740
Fully Specified Name
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
3
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.