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1 OMIM reference -
1 associated gene
7 signs/symptoms
COMMON GENES: 1
COMMON SIGNS: 3
1 OMIM reference -
1 associated gene
8 signs/symptoms
Brachydactyly-syndactyly, Zhao type
Syndactyly type 5

HOXD13 HOXD13


COMMON
GENES
HOXD13



Citations in the biomedical literature:


Brachydactyly-syndactyly, Zhao type
HOXD13
Syndactyly type 5



Brachydactyly-syndactyly, Zhao type
Syndactyly type 5

Synonym(s):
(no synonyms)

Synonym(s):
- Postaxial syndactyly with metacarpal synostosis
- SD5

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

External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: C538155


COMMON
SIGNS
- Autosomal dominant inheritance
- Metacarpal anomalies / Archibald's sign
- Syndactyly of toes


Brachydactyly-syndactyly, Zhao type
Syndactyly type 5

Very frequent
- Short foot / brachydactyly of toes
- Short hand / brachydactyly

Frequent
- Hallux valgus
- Symphalangy of fingers



Very frequent
- Terminal / third phalangeal bone of fingers hypoplasia
- Ulnar deviation of fingers

Frequent
- Camptodactyly of fingers
- Syndactyly of fingers / interdigital palm

Occasional
- Clinodactyly of fifth finger