Clinical Signs and Symptoms
ORPHA:166024 Multiple epiphyseal dysplasia, Al-Gazali type
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 skeletal system HP:0000924
- Clinodactyly HP:0030084
- Delayed epiphyseal ossification HP:0002663
- Enlarged joints HP:0003037
- Frontal bossing HP:0002007
- Genu valgum HP:0002857
- Hypertelorism HP:0000316
- Intellectual disability HP:0001249
- Macrocephaly HP:0000256
- Molar tooth sign on MRI HP:0002419
- Multiple epiphyseal dysplasia HP:0002654
- Pectus excavatum HP:0000767
- Spindle-shaped finger HP:0031092
- Triangular mouth HP:0000207
- Wide nasal bridge HP:0000431
Very frequent
- Agenesis of corpus callosum HP:0001274
- Arthralgia HP:0002829
- Hypoplasia of the corpus callosum HP:0002079
- Short stature HP:0004322
Frequent
- Cerebral atrophy HP:0002059
- Cutaneous syndactyly HP:0012725
Occasional
- Abnormal vertebral morphology HP:0003468
Rare
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.