Curry Jones syndrome

disorder

SNOMED 720819006CUI C0795915

Overview

Curry Jones 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.

2-3 finger osseus syndactyly

Very frequent (80-99%)HP:0025770

Cognitive delay

Very frequent (80-99%)HP:0001263

Hypopigmented skin patches

Very frequent (80-99%)HP:0001053

Increased distance between eyes

Very frequent (80-99%)HP:0000316

Partial syndactyly

Very frequent (80-99%)HP:0006101

3-4 toe syndactyly

Frequent (30-79%)HP:0009779

Abnormality of thumb phalanges

Frequent (30-79%)HP:0009602

Abnormally small eyeball

Frequent (30-79%)HP:0000568

Absence of corpus callosum

Frequent (30-79%)HP:0001274

Aplasia/Hypoplasia of the skin

Frequent (30-79%)HP:0008065

Broad thumbs

Frequent (30-79%)HP:0011304

Chronic constipation

Frequent (30-79%)HP:0012450

Craniosyostosis

Frequent (30-79%)HP:0001363

Dilated cerebral ventricle

Frequent (30-79%)HP:0002119

Duplication of phalanx of thumb

Frequent (30-79%)HP:0009942

Generalized hirsutism

Frequent (30-79%)HP:0002230

Hemimegalencephaly

Frequent (30-79%)HP:0007206

Low intelligence

Frequent (30-79%)HP:0001249

Polydactyly of the foot

Frequent (30-79%)HP:0001829

Preaxial polydactyly of foot

Frequent (30-79%)HP:0001841

Syndactyly of feet

Frequent (30-79%)HP:0001770

Unbalanced face

Frequent (30-79%)HP:0000324

Unilateral coronal craniosynostosis

Frequent (30-79%)HP:0011315

Arnold Chiari type I malformation

Occasional (5-29%)HP:0007099

Bilateral coronal suture craniosynostosis

Occasional (5-29%)HP:0011318

Enlarged brain

Occasional (5-29%)HP:0001355

Extra bones within cranial sutures

Occasional (5-29%)HP:0002645

High frontal hairline

Occasional (5-29%)HP:0009890

Hirsutism

Occasional (5-29%)HP:0001007

Intestinal malrotation

Occasional (5-29%)HP:0002566

Related Conditions

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

Aplasia of corpus callosum(parent)

Craniosynostosis syndrome(parent)

Polysyndactyly(parent)

Quick Facts

SNOMED CT: 720819006
UMLS CUI: C0795915
Fully Specified Name: Curry Jones syndrome (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.