ODCs

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

COMMON GENES: 1

2 OMIM references -
1 associated gene
4 signs/symptoms

Stapes ankylosis with broad thumbs and toes

Tarsal-carpal coalition syndrome

NOG

NOG

Citations in the biomedical literature:

Stapes ankylosis with broad thumbs and toes		Tarsal-carpal coalition syndrome
	Synonym(s): - Teunissen-Cremers syndrome		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic 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 dominant

	External references: 1 OMIM reference - No MeSH references		External references: 2 OMIM references - 1 MeSH reference: C536943

Tarsal-carpal coalition syndrome
	Very frequent - Ankle anomalies - Autosomal dominant inheritance - Short stature / dwarfism / nanism - Tarsal anomaly / fusion / synostosis
Stapes ankylosis with broad thumbs and toes
(no data available)