ODCs

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

PROTEIN INTERACTIONS: 1

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

Weissenbacher- Zweymuller syndrome

Spondyloepimetaphyseal dysplasia - short limb - abnormal calcification


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	COL11A2	(0.78)	DDR2

Citations in the biomedical literature:

Weissenbacher- Zweymuller syndrome		Spondyloepimetaphyseal dysplasia - short limb - abnormal calcification
	Synonym(s): - Heterozygous OSMED - Heterozygous otospondylomegaepiphyseal dysplasia - Pierre Robin sequence - fetal chondrodysplasia - Pierre Robin syndrome - fetal chondrodysplasia		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease - Rare maxillo-facial surgical disease - Rare otorhinolaryngologic 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: - Average age onset: - Average age of death: - Type of inheritance: autosomal recessive

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

No signs/symptoms info available.