Overview
Progeroid syndrome Petty 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.
Absent/underdeveloped tear glands
Always present (100%)HP:0008038
Birth weight less than 10th percentile
Always present (100%)HP:0001518
Craniosynostosis of coronal suture
Always present (100%)HP:0004440
Cryptorchidism
Always present (100%)HP:0000028
Decreased amniotic fluid index
Always present (100%)HP:0001562
Decreased projection of midface
Always present (100%)HP:0011800
Deformity of the skull
Always present (100%)HP:0001363
Down-slanting palpebral fissure
Always present (100%)HP:0000494
Hooked nose
Always present (100%)HP:0000444
Hypoplasia of supraorbital margins
Always present (100%)HP:0009891
Increased hair growth on body
Always present (100%)HP:0000998
Inverted triangular face
Always present (100%)HP:0000325
Premature skin wrinkling
Always present (100%)HP:0100678
Prominent veins
Always present (100%)HP:0001015
Short palpebral fissure
Always present (100%)HP:0012745
Wide cranium shape
Always present (100%)HP:0000248
Abnormal dermatoglyphics
Very frequent (80-99%)HP:0007477
Abnormal nail morphology
Very frequent (80-99%)HP:0001597
Abnormality of the hair shaft
Very frequent (80-99%)HP:0001595
Atrophy of fat
Very frequent (80-99%)HP:0100578
Brittle hair
Very frequent (80-99%)HP:0002299
Decreased body height
Very frequent (80-99%)HP:0004322
Decreased mineralization of skull
Very frequent (80-99%)HP:0004331
Dental agenesis
Very frequent (80-99%)HP:0009804
Dermal translucency
Very frequent (80-99%)HP:0010648
Distal phalangeal hypoplasia
Very frequent (80-99%)HP:0009882
Generalized hirsutism
Very frequent (80-99%)HP:0002230
Hypotrichosis
Very frequent (80-99%)HP:0008070
Increased width of the forehead
Very frequent (80-99%)HP:0000337
Intrauterine growth retardation, IUGR
Very frequent (80-99%)HP:0001511
Quick Facts
- SNOMED CT
- 770567006
- UMLS CUI
- C2676780
- Fully Specified Name
- Progeroid syndrome Petty 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.