Hallermann-Streiff syndrome

disorder

SNOMED 7903009CUI C0018522

Overview

Hallermann-Streiff 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.

Cataract, congenital

Very frequent (80-99%)HP:0000519

Decreased bone mineral density Z score

Very frequent (80-99%)HP:0004349

Decreased hair growth

Very frequent (80-99%)HP:0008070

Dental problems

Very frequent (80-99%)HP:0000164

Frontal protuberance

Very frequent (80-99%)HP:0002007

Hair loss

Very frequent (80-99%)HP:0001596

Hooked nose

Very frequent (80-99%)HP:0000444

Nanophthalmos

Very frequent (80-99%)HP:0000568

Rib exostoses

Very frequent (80-99%)HP:0000896

Short and broad skull

Very frequent (80-99%)HP:0000248

Short ribs

Very frequent (80-99%)HP:0000773

Short stature, proportionate

Very frequent (80-99%)HP:0003508

Skin degeneration

Very frequent (80-99%)HP:0004334

Sparse body hair

Very frequent (80-99%)HP:0002231

Abnormal cranial suture/fontanelle morphology

Frequent (30-79%)HP:0000235

Abnormality of hair volume

Frequent (30-79%)HP:0010719

Decreased projection of lower jaw

Frequent (30-79%)HP:0000347

Glossal abnormality

Frequent (30-79%)HP:0000157

Hypotrophic malar bone

Frequent (30-79%)HP:0000272

Impaired vision

Frequent (30-79%)HP:0000505

Increased intercanthal distance

Frequent (30-79%)HP:0000506

Increased tooth count

Frequent (30-79%)HP:0011069

Narrow mouth

Frequent (30-79%)HP:0000160

Natal tooth

Frequent (30-79%)HP:0000695

Retraction of the tongue

Frequent (30-79%)HP:0000162

Small nasal alae

Frequent (30-79%)HP:0000430

Thin eyelashes

Frequent (30-79%)HP:0000653

Varying degree of multiple fractures

Frequent (30-79%)HP:0002757

Abdominal situs inversus

Occasional (5-29%)HP:0003363

Abnormality of cardiovascular system morphology

Occasional (5-29%)HP:0030680

Related Conditions

Hypotrichosis(parent)

Multiple malformation syndrome, small stature, without skeletal dysplasia(parent)

Ectodermal dysplasia with hair-tooth defects(parent)

Genetic disease(parent)

Quick Facts

SNOMED CT: 7903009
UMLS CUI: C0018522
Fully Specified Name: Hallermann-Streiff 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.