Clinical Signs and Symptoms
ORPHA:1803 Thoracomelic dysplasia
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 fibula morphology HP:0002991
- Abnormality of pelvic girdle bone morphology HP:0002644
- Abnormality of the metaphysis HP:0000944
- Bell-shaped thorax HP:0001591
- Diaphyseal thickening HP:0005019
- Disproportionate short-limb short stature HP:0008873
- Elbow dislocation HP:0003042
- Flat face HP:0012368
- Genu valgum HP:0002857
- Hyperlordosis HP:0003307
- Joint hyperflexibility HP:0005692
- Limb undergrowth HP:0009826
- Low posterior hairline HP:0002162
- Narrow chest HP:0000774
- Round face HP:0000311
- Short ribs HP:0000773
Very frequent
- Gait disturbance HP:0001288
- Short neck HP:0000470
Occasional
Additional information
Further information
Specialised Social Services
Warning
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.