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Brachydactyly-syndactyly, Zhao type

1 OMIM reference -
1 associated gene
7 signs/symptoms

COMMON GENES: 1

Synpolydactyly type 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Brachydactyly-syndactyly, Zhao type

Synpolydactyly type 1

(UniProt - OMIM)

(UniProt - OMIM)


COMMON GENES	HOXD13

Citations in the biomedical literature:

Brachydactyly-syndactyly, Zhao type		Synpolydactyly type 1
	Synonym(s): (no synonyms)		Synonym(s): - SD2, Vordingborg type - SD2a - SPD, Vordingborg type - SPD1 - Synpolydactyly, Vordingborg type

	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: (no data available)

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

Brachydactyly-syndactyly, Zhao type
	Very frequent - Autosomal dominant inheritance - Metacarpal anomalies / Archibald's sign - Short foot / brachydactyly of toes - Short hand / brachydactyly - Syndactyly of toes Frequent - Hallux valgus - Symphalangy of fingers
Synpolydactyly type 1
(no data available)