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Curry-Hall syndrome

disorder
SNOMED 277807007CUI C0457013

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.

Abnormal toenail development
Very frequent (80-99%)HP:0100797
Abnormal toenail morphology
Very frequent (80-99%)HP:0008388
Abnormality of lingual frenum
Very frequent (80-99%)HP:0000190
Abnormality of the fingernails
Very frequent (80-99%)HP:0001231
Dental problems
Very frequent (80-99%)HP:0000164
Dystrophic nails
Very frequent (80-99%)HP:0008404
Hypoplastic toenails
Very frequent (80-99%)HP:0001800
Missing between one and six teeth
Very frequent (80-99%)HP:0000668
Peg-shaped teeth
Very frequent (80-99%)HP:0000698
Postaxial hand polydactyly
Very frequent (80-99%)HP:0001162
Premature tooth eruption
Very frequent (80-99%)HP:0006288
short stature, mild
Very frequent (80-99%)HP:0003502
Single median incisor
Very frequent (80-99%)HP:0006315
Small nail
Very frequent (80-99%)HP:0001792
Abnormal antihelix morphology
Frequent (30-79%)HP:0009738
Disproportionately small hands
Frequent (30-79%)HP:0200055
Overlapping fingers
Frequent (30-79%)HP:0010557
Permanent curving of the pinkie finger
Frequent (30-79%)HP:0004209
Tessier cleft
Frequent (30-79%)HP:0002006
Brachydactyly
HP:0001156
Fibular polydactyly
HP:0001830
Nail dysplasia
HP:0002164
Ocular hypotelorism
HP:0000601
Prominent antihelix
HP:0000395
Short hands
HP:0004279

Quick Facts

SNOMED CT
277807007
UMLS CUI
C0457013
Fully Specified Name
Curry-Hall syndrome (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
25
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.