Overview
Progressive hemifacial atrophy 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 mandible morphology
Very frequent (80-99%)HP:0000277
Decreased projection of lower jaw
Very frequent (80-99%)HP:0000347
Irregular hyperpigmentation
Very frequent (80-99%)HP:0007400
Unbalanced face
Very frequent (80-99%)HP:0000324
Aplasia/Hypoplasia of the skin
Frequent (30-79%)HP:0008065
Epilepsy
Frequent (30-79%)HP:0001250
Muscular abnormality
Frequent (30-79%)HP:0003011
Uneven or disproportionate growth of one body part compared to another
Frequent (30-79%)HP:0100555
Deep set eye
Occasional (5-29%)HP:0000490
Eyelid ptosis
Occasional (5-29%)HP:0000508
Heterochromia iridis
Occasional (5-29%)HP:0001100
Alopecia areata
HP:0002232
Angle class 3 malocclusion
HP:0000689
Ataxia
HP:0001251
Atrophy of half of face
HP:0011331
Blepharophimosis
HP:0000581
Decreased size of mandibular ramus
HP:0003778
Delayed eruption of teeth
HP:0000684
Horner syndrome
HP:0002277
Hunched back
HP:0002808
Intermittent migraine headaches
HP:0002076
Microtia
HP:0008551
Patch of white hair
HP:0002290
Trigeminal neuralgia
HP:0100661
Wasting of the tongue
HP:0012473
Related Conditions
Quick Facts
- SNOMED CT
- 718224004
- UMLS CUI
- C0015458
- Fully Specified Name
- Progressive hemifacial atrophy (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 25
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.