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Synpolydactyly type 1

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

COMMON GENES: 1

Syndactyly type 5

1 OMIM reference -
1 associated gene
8 signs/symptoms

Synpolydactyly type 1

Syndactyly type 5

(UniProt - OMIM)

(UniProt - OMIM)


COMMON GENES	HOXD13

Citations in the biomedical literature:

Synpolydactyly type 1		Syndactyly type 5
	Synonym(s): - SD2, Vordingborg type - SD2a - SPD, Vordingborg type - SPD1 - Synpolydactyly, Vordingborg type		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: (no data available)		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

Syndactyly type 5
	Very frequent - Autosomal dominant inheritance - Metacarpal anomalies / Archibald's sign - Terminal / third phalangeal bone of fingers hypoplasia - Ulnar deviation of fingers Frequent - Camptodactyly of fingers - Syndactyly of fingers / interdigital palm - Syndactyly of toes Occasional - Clinodactyly of fifth finger
Synpolydactyly type 1
(no data available)