Symphalangism Cushing type

disorder

SNOMED 1162837001CUI C1861385

Overview

Symphalangism Cushing 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.

Cushing's symphalangism

Very frequent (80-99%)HP:0100264

Fusion of wrist bones

Very frequent (80-99%)HP:0005048

Proximal interphalangeal finger joint contractures

Very frequent (80-99%)HP:0100490

Tarsal bone synostosis

Very frequent (80-99%)HP:0008368

Abnormal metacarpal morphology

Frequent (30-79%)HP:0005916

Brachydactyly

Frequent (30-79%)HP:0001156

Curvature of finger

Frequent (30-79%)HP:0040019

Elbow ankylosis

Frequent (30-79%)HP:0003070

Fused long bone of hand with innermost finger bone

Frequent (30-79%)HP:0005880

Radiohumeral dislocation

Frequent (30-79%)HP:0003042

Sensorineural deafness

Frequent (30-79%)HP:0000407

Abnormality of the wrist

Occasional (5-29%)HP:0003019

Partial syndactyly

Occasional (5-29%)HP:0006101

Permanent curving of the pinkie finger

Occasional (5-29%)HP:0004209

Squint

Occasional (5-29%)HP:0000486

Related Conditions

Autosomal dominant hereditary disorder(parent)

Proximal interphalangeal joint symphalangism(parent)

Developmental hereditary disorder(parent)

Hereditary disorder of musculoskeletal system(parent)

Quick Facts

SNOMED CT: 1162837001
UMLS CUI: C1861385
Fully Specified Name: Proximal interphalangeal joint symphalangism Cushing type (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 15

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.