Symphalangism with multiple anomalies of hands and feet

disorder

SNOMED 732955001CUI C1861391

Overview

Symphalangism with multiple anomalies of hands and feet 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.

Decreased space in hinge joint

Very frequent (80-99%)HP:0006019

Symphalangism of the 4th finger

Very frequent (80-99%)HP:0004197

Symphalangism of the 5th finger

Very frequent (80-99%)HP:0004218

Abnormal dermatoglyphics

Frequent (30-79%)HP:0007477

Abnormality of the distal phalanges of the toes

Frequent (30-79%)HP:0010182

Absent outermost hand bone

Frequent (30-79%)HP:0009881

Aplasia of the distal interphalangeal creases

Frequent (30-79%)HP:0001032

Brachydactyly

Frequent (30-79%)HP:0001156

Curvature of digit

Frequent (30-79%)HP:0030084

Decreased thenar eminence

Frequent (30-79%)HP:0001245

Large head

Frequent (30-79%)HP:0000256

Partial syndactyly

Frequent (30-79%)HP:0006101

Small hypothenar eminence

Frequent (30-79%)HP:0010487

Symphalangism affecting the phalanges of the toes

Frequent (30-79%)HP:0010179

Symphalangism of the hand

Frequent (30-79%)HP:0009700

Syndactyly of feet

Frequent (30-79%)HP:0001770

Abnormal finger flexion crease

Occasional (5-29%)HP:0006143

Abnormal palmar dermatoglyphics

Occasional (5-29%)HP:0001018

Absent/small outermost pinky toe bone

Occasional (5-29%)HP:0100371

Cutaneous syndactyly between fingers 2 and 5

Occasional (5-29%)HP:0005650

Hearing loss, conductive

Occasional (5-29%)HP:0000405

Small outermost bone of big toe

Occasional (5-29%)HP:0010103

Related Conditions

Autosomal dominant hereditary disorder(parent)

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

Symphalangism(parent)

Hereditary disorder of musculoskeletal system(parent)

Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT: 732955001
UMLS CUI: C1861391
Fully Specified Name: Symphalangism with multiple anomalies of hands and feet syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 22

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.