Cooks syndrome

disorder

SNOMED 720747002CUI C1862841

Overview

Cooks 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.

Aplastic/hypoplastic toenails

Very frequent (80-99%)HP:0010624

Brachydactyly

Very frequent (80-99%)HP:0001156

Broad thumbs

Very frequent (80-99%)HP:0011304

Dystrophic fingernails

Very frequent (80-99%)HP:0008391

Dystrophic toenails

Very frequent (80-99%)HP:0001810

Split hand

Very frequent (80-99%)HP:0001171

Triphalangy of thumb

Very frequent (80-99%)HP:0001199

Abnormal toenail morphology

Frequent (30-79%)HP:0008388

Anonychia

HP:0001798

Complete duplication of thumb bones

HP:0009943

Convex bridge of nose

HP:0000426

Decreased height of philtrum

HP:0000322

Down-slanting palpebral fissure

HP:0000494

Dystrophic nails

HP:0008404

High arched palate

HP:0000218

Hypoplastic/small little finger

HP:0009237

Nail dysplasia

HP:0002164

Nasal hypertrophy

HP:0000448

Shortening of all outermost bone of the toes

HP:0005793

Shortening of all outermost bones of the fingers

HP:0006118

Small nasal alae

HP:0000430

Related Conditions

Autosomal dominant hereditary disorder(parent)

Congenital anomaly of nail(parent)

Multiple malformation syndrome with limb defect as major feature(parent)

Brachydactyly(parent)

Hereditary disorder of the integument(parent)

Genetic disorder of nail(parent)

Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT: 720747002
UMLS CUI: C1862841
Fully Specified Name: Cooks syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 21

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.