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1 OMIM reference -
1 associated gene
9 signs/symptoms
COMMON GENES: 1
COMMON SIGNS: 1
3 OMIM references -
3 associated genes
10 signs/symptoms
Angel-shaped phalango-epiphyseal dysplasia
Multiple synostoses syndrome

GDF5 FGF9
GDF5
NOG


COMMON
GENES
GDF5



Citations in the biomedical literature:


Angel-shaped phalango-epiphyseal dysplasia
GDF5
Multiple synostoses syndrome
FGF9 NOG



Angel-shaped phalango-epiphyseal dysplasia
Multiple synostoses syndrome

Synonym(s):
- ASPED

Synonym(s):
- Deafness - symphalangism syndrome, Hermann type
- Facio-audio-symphalangism
- Symphalangism - brachydactyly
- WL syndrome

Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare otorhinolaryngologic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
No MeSH references
External references:
3 OMIM references -
No MeSH references


COMMON
SIGNS
- Autosomal dominant inheritance


Angel-shaped phalango-epiphyseal dysplasia
Multiple synostoses syndrome

Very frequent
- Epiphyseal anomaly

Frequent
- Anomalies of teeth and dentition
- Arthritis / synovitis / synovial proliferation
- Delayed dentition / eruption of teeth / lack of eruption of teeth
- Hip dislocation / dysplasia / coxa valga / coxa vara / coxa plana
- Short stature / dwarfism / nanism

Occasional
- Delayed bone age
- Hyperextensible joints / articular hyperlaxity


Very frequent
- Conductive deafness / hearing loss
- Restricted joint mobility / joint stiffness / ankylosis
- Short hand / brachydactyly
- Symphalangy of fingers

Frequent
- Broad / bifid thumb
- Cone epiphyses / epiphysis
- Simian crease / transverse / unique palmar crease

Occasional
- Facial structural asymmetry / facial hemiatrophy / facial hemihypertrophy
- Nails anomalies