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1 OMIM reference -
2 associated genes
11 signs/symptoms
PROTEIN INTERACTIONS: 1
3 associated genes
No signs/symptoms info
Brachydactyly type C
Dedifferentiated liposarcoma

BMPR1B CDK4
GDF5 HMGA2
MDM2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
BMPR1B
(0.52)
CDK4



Citations in the biomedical literature:


Brachydactyly type C
BMPR1B GDF5
Dedifferentiated liposarcoma
CDK4 HMGA2 MDM2



Brachydactyly type C
Dedifferentiated liposarcoma

Synonym(s):
(no synonyms)

Synonym(s):
- DDLS

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

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

Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: adult
Type of inheritance: sporadic

External references:
1 OMIM reference -
1 MeSH reference: C537093
External references:
No OMIM references
No MeSH references

Brachydactyly type C

Very frequent
- Autosomal dominant inheritance
- Metacarpal anomalies / Archibald's sign
- Short hand / brachydactyly
- Ulnar deviation of fingers

Frequent
- Cone epiphyses / epiphysis
- Short foot / brachydactyly of toes
- Thin / hypoplastic / hyperconvex fingernails

Occasional
- Clinodactyly of fifth finger
- Short stature / dwarfism / nanism
- Symphalangy of fingers
- Talipes-valgus


Dedifferentiated liposarcoma

(no data available)