Overview
Acrodysostosis 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
Abnormal vertebral bodies
Very frequent (80-99%)HP:0003312
Brachydactyly
Very frequent (80-99%)HP:0001156
Broad flat nasal bridge
Very frequent (80-99%)HP:0000431
Concave bridge of nose
Very frequent (80-99%)HP:0005280
Cone-shaped epiphyses
Very frequent (80-99%)HP:0010579
Decreased body height
Very frequent (80-99%)HP:0004322
Deficiency of upper jaw bones
Very frequent (80-99%)HP:0000327
Early bone maturation
Very frequent (80-99%)HP:0005616
Flat midface
Very frequent (80-99%)HP:0011800
Mental deficiency
Very frequent (80-99%)HP:0001249
Nail disease
Very frequent (80-99%)HP:0001597
Nasal hypoplasia
Very frequent (80-99%)HP:0003196
Retruded nasal dorsum
Very frequent (80-99%)HP:0000457
Short long bone of foot
Very frequent (80-99%)HP:0010743
Short toes
Very frequent (80-99%)HP:0001831
Shortened long bones of hand
Very frequent (80-99%)HP:0010049
Slack jawed appearance
Very frequent (80-99%)HP:0000194
Stippling of the epiphyses
Very frequent (80-99%)HP:0010655
Abnormal female external genitalia
Frequent (30-79%)HP:0000055
Abnormal metaphysis morphology
Frequent (30-79%)HP:0000944
Abnormal morphology of the radius
Frequent (30-79%)HP:0002818
Abnormal morphology of ulna
Frequent (30-79%)HP:0040071
Abnormal shape of shaft of long bone
Frequent (30-79%)HP:0000940
Abnormality of immune system physiology
Frequent (30-79%)HP:0010978
Abnormality of the thighbone
Frequent (30-79%)HP:0002823
Bowed long bones
Frequent (30-79%)HP:0006487
Bulging forehead
Frequent (30-79%)HP:0011220
Cone-shaped metacarpal epiphyses
Frequent (30-79%)HP:0006059
Cryptorchidism
Frequent (30-79%)HP:0000028
Related Conditions
Acromesomelic dysplasia syndrome(parent)
Autosomal dominant hereditary disorder(parent)
Hereditary disorder of musculoskeletal system(parent)
Dysostosis(parent)
Longitudinal deficiency of foot(parent)
Congenital undergrowth of partial lower limb(parent)
Longitudinal deficiency of part of upper limb(parent)
Developmental hereditary disorder(parent)
Congenital deformity of hand(parent)
Congenital dysplasia of lower extremity(parent)
Quick Facts
- SNOMED CT
- 66758006
- UMLS CUI
- C0220659
- Fully Specified Name
- Acrodysostosis (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.