Mirror hands and feet co-occurrent with nasal defect

disorder

SNOMED 715440003CUI C1851100

Overview

Mirror hands and feet co-occurrent with nasal defect 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.

Abnormal metacarpal morphology

Very frequent (80-99%)HP:0005916

Aplastic/hypoplastic thumbs

Very frequent (80-99%)HP:0009601

Mirror image polydactyly

Very frequent (80-99%)HP:0010689

Partial syndactyly

Very frequent (80-99%)HP:0006101

Preaxial hand polydactyly

Very frequent (80-99%)HP:0001177

Preaxial polydactyly of foot

Very frequent (80-99%)HP:0001841

Syndactyly of feet

Very frequent (80-99%)HP:0001770

Tarsal bone synostosis

Very frequent (80-99%)HP:0008368

Triphalangy of thumb

Very frequent (80-99%)HP:0001199

Abnormality of the wrist

Frequent (30-79%)HP:0003019

Absent shinbone

Frequent (30-79%)HP:0009556

Dimelia

Frequent (30-79%)HP:0100524

Fibular duplication

Frequent (30-79%)HP:0010503

Hypoplasia of columella

Frequent (30-79%)HP:0002000

Large nose

Frequent (30-79%)HP:0000448

Limitation of joint mobility

Frequent (30-79%)HP:0001376

Nasal deformity

Frequent (30-79%)HP:0000366

Radial aplasia

Frequent (30-79%)HP:0003974

Retruded nasal dorsum

Frequent (30-79%)HP:0000457

Small nasal alae

Frequent (30-79%)HP:0000430

Talipes

Frequent (30-79%)HP:0001883

Central hypotonia

Occasional (5-29%)HP:0001252

Cryptorchidism

Occasional (5-29%)HP:0000028

Downturned corners of mouth

Occasional (5-29%)HP:0002714

Dull intelligence

Occasional (5-29%)HP:0001249

Hypoplastic or absent corpus callosum

Occasional (5-29%)HP:0007370

Increased distance between eyes

Occasional (5-29%)HP:0000316

Nonsyndromal hydrocephalus

Occasional (5-29%)HP:0000238

Anomaly of the face

HP:0000271

Broad foot

HP:0001769

Related Conditions

Autosomal dominant hereditary disorder(parent)

Polysyndactyly(parent)

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

Congenital anomaly of nose(parent)

Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT: 715440003
UMLS CUI: C1851100
Fully Specified Name: Mirror hands and feet co-occurrent with nasal defect (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.