← Back to Conditions

Hay-Wells syndrome of ectodermal dysplasia

disorder
SNOMED 55821006CUI C0406709

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.

Absent tear secretion
Always present (100%)HP:0000522
Bilateral blockage of the rear opening of the nasal cavity
Always present (100%)HP:0004502
Dystrophic nails
Always present (100%)HP:0008404
Ectodermal dysplasia
Always present (100%)HP:0000968
Pili torti
Always present (100%)HP:0003777
Sparse body hair
Always present (100%)HP:0002231
Sweating dysfunction
Always present (100%)HP:0000970
Ankyloblepharon filiforme adnatum
Very frequent (80-99%)HP:0009755
Broad flat nasal bridge
Very frequent (80-99%)HP:0000431
Cleft of upper lip
Very frequent (80-99%)HP:0000204
Coarse hair texture
Very frequent (80-99%)HP:0002208
Decreased sweating
Very frequent (80-99%)HP:0000966
Dystrophic fingernails
Very frequent (80-99%)HP:0008391
Dystrophic toenails
Very frequent (80-99%)HP:0001810
Hearing loss, conductive
Very frequent (80-99%)HP:0000405
Hypotrichosis
Very frequent (80-99%)HP:0008070
Lacrimal duct atresia
Very frequent (80-99%)HP:0000564
Nail overcurvature
Very frequent (80-99%)HP:0001795
Non-midline cleft of the upper lip
Very frequent (80-99%)HP:0100335
Tubular fingernails
Very frequent (80-99%)HP:0001812
Cleft lip
Frequent (30-79%)HP:0410030
Cleft of palate
Frequent (30-79%)HP:0000175
Dystrophic tooth enamel
Frequent (30-79%)HP:0000682
Generalised hyperpigmentation
Frequent (30-79%)HP:0007440
Hypoplastic mandible condyle
Frequent (30-79%)HP:0000347
Hypospadias
Frequent (30-79%)HP:0000047
Keratoderma
Frequent (30-79%)HP:0000982
Missing between one and six teeth
Frequent (30-79%)HP:0000668
Nasogastric tube feeding in infancy
Frequent (30-79%)HP:0011470
Pointed tooth
Frequent (30-79%)HP:0000698

Related Conditions

Ectodermal dysplasia with hair-tooth-nail-sweating defect(parent)
Multiple malformation syndrome with facial-limb defects as major feature(parent)
Skin lesion(parent)

Quick Facts

SNOMED CT
55821006
UMLS CUI
C0406709
Fully Specified Name
Hay-Wells syndrome of ectodermal dysplasia (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
30
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.