ODCs

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1 OMIM reference -
2 associated genes
10 signs/symptoms

COMMON GENES: 2
COMMON SIGNS: 6

1 OMIM reference -
2 associated genes
14 signs/symptoms

Syndactyly type 4

Hypoplastic tibiae - postaxial polydactyly

LMBR1	(UniProt - OMIM)		LMBR1	(UniProt - OMIM)
SHH	(UniProt - OMIM)		SHH	(UniProt - OMIM)

Citations in the biomedical literature:

Syndactyly type 4		Hypoplastic tibiae - postaxial polydactyly
	Synonym(s): - Polysyndactyly, Haas type		Synonym(s): - Werner mesomelic 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: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown 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 - No MeSH references


COMMON SIGNS	- Autosomal dominant inheritance - Complete claw hand / camptodactyly of all fingers - Fingerlike / triphalangeal thumb - Restricted joint mobility / joint stiffness / ankylosis - Syndactyly of fingers / interdigital palm - Tibia anomaly (excluding short) / absence / agenesis / hypoplasia / tibial ray anomaly

Syndactyly type 4		Hypoplastic tibiae - postaxial polydactyly
	Very frequent - Upper limb polydactyly / hexadactyly Frequent - Metacarpal anomalies / Archibald's sign - Polydactyly of toes - Syndactyly of toes		Very frequent - Bowed diaphysis / diaphyses / long bones - Clinodactyly of fifth finger - Fibula anomaly (excluding short) / absence / agenesis / hypoplasia / fibular ray anomaly - Postaxial polydactyly (hand) Frequent - Preaxial polydactyly (hand) Occasional - Short columella / depressed nasal tip - Short stature / dwarfism / nanism - Thumb hypoplasia / aplasia / absence