ODCs

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1 OMIM reference -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

2 OMIM references -
3 associated genes
11 signs/symptoms

Oculootodental syndrome

Autosomal recessive hypohidrotic ectodermal dysplasia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FADD	(0.63)	EDAR

Citations in the biomedical literature:

Oculootodental syndrome		Autosomal recessive hypohidrotic ectodermal dysplasia
	Synonym(s): - OOD		Synonym(s): - AR-HED - Autosomal recessive anhidrotic ectodermal dysplasia

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare odontologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic disease - Rare skin disease

	Classification (ICD10): - Diseases of the digestive system -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: no data available Type of inheritance: autosomal recessive

	External references: 1 OMIM reference - No MeSH references		External references: 2 OMIM references - 1 MeSH reference: D053360

Autosomal recessive hypohidrotic ectodermal dysplasia
	Very frequent - Abnormal fingernails - Abnormal toenails - Anodontia / oligodontia / hypodontia - Autosomal recessive inheritance - Dry / squaly skin / exfoliation - Fine hair - Hair and scalp anomalies - Premature lost of decidious teeth Frequent - Alopecia - Hypohidrosis / decreased sweating / thermoregulation disorder / heat intolerance - Tooth shape anomaly
Oculootodental syndrome
(no data available)