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Radial hemimelia, bilateral

2 associated genes
No signs/symptoms info

COMMON GENES: 2

Syndactyly type 4

1 OMIM reference -
2 associated genes
10 signs/symptoms

Radial hemimelia, bilateral

Syndactyly type 4

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


COMMON GENES	LMBR1 SHH

Citations in the biomedical literature:

Radial hemimelia, bilateral		Syndactyly type 4
	Synonym(s): - Radial longitidinal meromelia, bilateral		Synonym(s): - Polysyndactyly, Haas 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: (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: No OMIM references No MeSH references		External references: 1 OMIM reference - No MeSH references

Syndactyly type 4
	Very frequent - Autosomal dominant inheritance - Complete claw hand / camptodactyly of all fingers - Syndactyly of fingers / interdigital palm - Upper limb polydactyly / hexadactyly Frequent - Metacarpal anomalies / Archibald's sign - Polydactyly of toes - Syndactyly of toes - Tibia anomaly (excluding short) / absence / agenesis / hypoplasia / tibial ray anomaly Occasional - Fingerlike / triphalangeal thumb - Restricted joint mobility / joint stiffness / ankylosis
Radial hemimelia, bilateral
(no data available)