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1 OMIM reference -
1 associated gene
9 signs/symptoms
COMMON GENES: 1
COMMON SIGNS: 3
1 OMIM reference -
1 associated gene
15 signs/symptoms
Angel-shaped phalango-epiphyseal dysplasia
Fibular aplasia - complex brachydactyly

GDF5 GDF5


COMMON
GENES
GDF5



Citations in the biomedical literature:


Angel-shaped phalango-epiphyseal dysplasia
GDF5
Fibular aplasia - complex brachydactyly



Angel-shaped phalango-epiphyseal dysplasia
Fibular aplasia - complex brachydactyly

Synonym(s):
- ASPED

Synonym(s):
- Du Pan 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

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: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive

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


COMMON
SIGNS
- Epiphyseal anomaly
- Hip dislocation / dysplasia / coxa valga / coxa vara / coxa plana
- Short stature / dwarfism / nanism


Angel-shaped phalango-epiphyseal dysplasia
Fibular aplasia - complex brachydactyly

Very frequent
- Autosomal dominant inheritance

Frequent
- Anomalies of teeth and dentition
- Arthritis / synovitis / synovial proliferation
- Delayed dentition / eruption of teeth / lack of eruption of teeth

Occasional
- Delayed bone age
- Hyperextensible joints / articular hyperlaxity


Very frequent
- Autosomal recessive inheritance
- Carpal bones fusion / synostosis
- Narrow nasal bridge
- Radius anomaly / absence / agenesis / hypoplasia / abnormal radial ray
- Restricted joint mobility / joint stiffness / ankylosis
- Short hand / brachydactyly
- Short limbs / micromelia / brachymelia
- Simian crease / transverse / unique palmar crease
- Tarsal anomaly / fusion / synostosis
- Thumb anomalies (excluding hypoplasia)
- Tibia anomaly (excluding short) / absence / agenesis / hypoplasia / tibial ray anomaly
- Ulnar / cubital anomaly / absence / agenesis / hypoplasia / abnormal ulnar / cubital ray