Clinical Signs and Symptoms
ORPHA:56305 Atelosteogenesis type III
The phenotypic description of this disease is based on an analysis of the biomedical literature and uses the terms of the Human Phenotype Ontology (HPO). Phenotypic abnormalities are presented by order of frequency of occurrence in the patient population, then by alphabetical order inside each frequency group.
- Abnormality of the humerus HP:0003063
- Coronal cleft vertebrae HP:0003417
- Distal tapering femur HP:0006408
- Elbow dislocation HP:0003042
- Hip dislocation HP:0002827
- Knee dislocation HP:0004976
- Patellar dislocation HP:0002999
- Respiratory insufficiency HP:0002093
- Short tubular bones of the hand HP:0001248
- Talipes equinovarus HP:0001762
- Vertebral hypoplasia HP:0008417
- Abnormal cervical curvature HP:0005905
- Absent humerus HP:0003862
- Absent radius HP:0003974
- Club-shaped distal femur HP:0006384
- Epiphyseal stippling of the humerus HP:0003902
- Fibular aplasia HP:0002990
- Global developmental delay HP:0001263
- Hand clenching HP:0001188
- High palate HP:0000218
- Laryngotracheomalacia HP:0008755
- Micrognathia HP:0000347
- Polyhydramnios HP:0001561
- Short tibia HP:0005736
- Thoracic hypoplasia HP:0005257
- Thoracolumbar kyphosis HP:0005619
- Ulnar deviation of the wrist HP:0003049
Specialised Social Services
The information provided is based on published scientific articles.
The information provided is estimated for the entire population of patients in routine care. Some phenotypic abnormalities reported here may occur individually with a variable temporality or severity, while others, not listed, may still be encountered. Phenotypic annotations are not yet available for all rare diseases; the annotation process is ongoing.
The information contained in Orphanet is regularly updated. It is possible that discoveries have been made since the last update and have not yet been incorporated.
Professionals are encouraged to always consult the latest scientific publications before making a decision based on the information provided. The information contained in Orphanet is not intended to replace the services of a healthcare professional. Orphanet cannot be held responsible for the deleterious, truncated or erroneous use of any information found in the Orphanet database.