Metaphyseal dysplasia Braun Tinschert type

disorder

SNOMED 717221005CUI C1853825

Overview

Metaphyseal dysplasia Braun Tinschert 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.

Advanced pneumatization of cranial sinuses

Frequent (30-79%)HP:0010540

Bipartite patella

Frequent (30-79%)HP:0010498

Broad femoral neck

Frequent (30-79%)HP:0006429

Broad radial metaphysis

Frequent (30-79%)HP:0004026

Broad tibial metaphyses

Frequent (30-79%)HP:0006413

Coarse metaphyseal trabecularization

Frequent (30-79%)HP:0100670

Deformed humerus

Frequent (30-79%)HP:0003871

Elevated alkaline phosphatase of bone origin

Frequent (30-79%)HP:0010639

Exostoses of the radius

Frequent (30-79%)HP:0003986

Exostoses of the ulna

Frequent (30-79%)HP:0003985

Fibular bowing

Frequent (30-79%)HP:0010502

Flared metaphysis of thigh bone

Frequent (30-79%)HP:0002834

Humerus varus

Frequent (30-79%)HP:0003874

Hypoplasia of the ulna

Frequent (30-79%)HP:0003022

Increased bone density in innermost finger bone

Frequent (30-79%)HP:0100917

Increased bone mineral density

Frequent (30-79%)HP:0011001

Increased urinary type 1 collagen N-terminal telopeptide level

Frequent (30-79%)HP:0032208

Radial bowing

Frequent (30-79%)HP:0002986

Sclerosis of middle finger phalanx

Frequent (30-79%)HP:0100916

Skeletal dysplasia

Frequent (30-79%)HP:0002652

Thin cortices

Frequent (30-79%)HP:0002753

Tibial bowing

Frequent (30-79%)HP:0002982

Ulnar bowing

Frequent (30-79%)HP:0003031

Upper limb metaphyseal widening

Frequent (30-79%)HP:0003856

Wide distal femoral metaphysis

Frequent (30-79%)HP:0006387

Wide head of thigh bone

Frequent (30-79%)HP:0008804

Wide metaphysis of innermost thighbone

Frequent (30-79%)HP:0008783

Widened long bones

Frequent (30-79%)HP:0005622

Osteopenia

Occasional (5-29%)HP:0000938

Premature exfoliation of primary teeth

Occasional (5-29%)HP:0006323

Related Conditions

Autosomal dominant hereditary disorder(parent)

Dysplasia with increased bone density(parent)

Hereditary disorder of musculoskeletal system(parent)

Congenital anomaly of skeletal bone(parent)

Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT: 717221005
UMLS CUI: C1853825
Fully Specified Name: Metaphyseal dysplasia Braun Tinschert type (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.