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Hypotrichosis and intellectual disability syndrome Lopes type

disorder
SNOMED 723365002CUI C4509839

Overview

Hypotrichosis and intellectual disability syndrome Lopes type 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.

1-5 finger complete cutaneous syndactyly
Frequent (30-79%)HP:0006088
Hypotrichosis
Frequent (30-79%)HP:0008070
Low intelligence
Frequent (30-79%)HP:0001249
Premature tooth eruption
Frequent (30-79%)HP:0006288

Related Conditions

Congenital hypotrichia(parent)
Recessive hereditary disorder (autosomal)(parent)
Hereditary disorder of the integument(parent)
Syndactyly(parent)
Developmental hereditary disorder(parent)
Genetic intellectual disability(parent)

Quick Facts

SNOMED CT
723365002
UMLS CUI
C4509839
Fully Specified Name
Hypotrichosis and intellectual disability syndrome Lopes type (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
4
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.