Ectodermal dysplasia trichoodontoonychial type

disorder

SNOMED 734018003CUI C1851858

Overview

Ectodermal dysplasia trichoodontoonychial 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.

Abnormal toenail morphology

Very frequent (80-99%)HP:0008388

Atrophy of fat

Very frequent (80-99%)HP:0100578

Decreased hair growth

Very frequent (80-99%)HP:0008070

Irregular hyperpigmentation of back

Very frequent (80-99%)HP:0007521

Misshapened teeth

Very frequent (80-99%)HP:0006482

Missing between one and six teeth

Very frequent (80-99%)HP:0000668

Nasal anomaly

Very frequent (80-99%)HP:0000366

Sparse body hair

Very frequent (80-99%)HP:0002231

Abnormality of the eyelashes

Frequent (30-79%)HP:0000499

Absence of eyebrow

Frequent (30-79%)HP:0100840

Aplasia/Hypoplasia of the nipples

Frequent (30-79%)HP:0006709

Noncancerous mole

Frequent (30-79%)HP:0000995

Related Conditions

Autosomal dominant hereditary disorder(parent)

Ectodermal dysplasia with hair-tooth-nail defects(parent)

Hereditary disorder of the integument(parent)

Genetic disorder of nail(parent)

Developmental hereditary disorder(parent)

Hereditary disorder of tooth(parent)

Partial congenital absence of teeth(parent)

Quick Facts

SNOMED CT: 734018003
UMLS CUI: C1851858
Fully Specified Name: Ectodermal dysplasia trichoodontoonychial type (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.