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Otodental syndrome

1 OMIM reference -
1 associated gene
25 signs/symptoms

PROTEIN INTERACTIONS: 1
COMMON SIGNS: 2

Septo-optic dysplasia

1 OMIM reference -
6 associated genes
34 signs/symptoms

Otodental syndrome

Septo-optic dysplasia

FGF3	(UniProt - OMIM)		FGFR1	(UniProt - OMIM)
			HESX1	(UniProt - OMIM)
			OTX2	(UniProt - OMIM)
			PROKR2	(UniProt - OMIM)
			SOX2	(UniProt - OMIM)
			SOX3	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FGF3	(0.52)	FGFR1

Citations in the biomedical literature:

Otodental syndrome		Septo-optic dysplasia
	Synonym(s): - Globodontia - Otodental dysplasia		Synonym(s): - De Morsier syndrome - SOD - Septo-optic dysplasia spectrum

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

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

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood 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 - 1 MeSH reference: D025962


COMMON SIGNS	- Autosomal dominant inheritance - Sensorineural deafness / hearing loss

Otodental syndrome		Septo-optic dysplasia
	Very frequent - Tooth shape anomaly Frequent - Anodontia / oligodontia / hypodontia - Broad cheeks / cherub-like / cherubin face - Delayed dentition / eruption of teeth / lack of eruption of teeth - Dental malocclusion - Enamel anomaly - Long face - Taurodontia - Thickened / hypertrophic / fibromatous gingivae Occasional - Anophthalmos / anophthalmia / microphthalmos / microphthalmia - Anteverted nares / nostrils - Cataract / lens opacification - Coloboma of iris - Coloboma of the lens - Heterochromia / mixed colouring of iris - High vaulted / narrow palate - Long philtrum - Microcornea - Micrognathia / retrognathia / micrognathism / retrognathism - Pigmented naevi / naevus pigmentosus / lentigo - Prominent / bat ears - Retinoschisis / retinal / chorioretinal coloboma - Supernumerary teeth / polyodontia		Very frequent - Optic nerve anomaly / optic atrophy / anomaly of the papilla - Septo-optic dysplasia - Visual loss / blindness / amblyopia Frequent - Cleft palate without cleft lip / submucosal cleft palate / bifid uvula - Corpus callosum / septum pellucidum total / partial agenesis - Hemiplegia / diplegia / hemiparesia / limb palsy - Hypothalamic-hypophyseal axis anomalies / hypothalamus / pituitary anomalies - Hypothalamic-hypophyseal axis functional anomalies / hypopituitarism - Micropenis / small penis / agenesis - Nystagmus - Seizures / epilepsy / absences / spasms / status epilepticus - Short stature / dwarfism / nanism - Strabismus / squint - Undescended / ectopic testes / cryptorchidia / unfixed testes Occasional - Anosmia / cacosmia / hypogeusia / hyposmia / olfactory bulb hypoplasia - Antenatal exposure : alcohol - Asthenia / fatigue / weakness - Autism / autistic disoders - Autosomal recessive inheritance - Cerebellum / cerebellar vermis anomaly / agenesis / hypoplasia - Congenital cardiac anomaly / malformation / cardiopathy - Constipation - Diabetes insipidus - Dry / squaly skin / exfoliation - Generalized obesity - Hypohidrosis / decreased sweating / thermoregulation disorder / heat intolerance - Intellectual deficit / mental / psychomotor retardation / learning disability - Maternal diabetes - Pollakiuria / polyuria / dysuria / anuria / acute urine retention / oliguria - Sleep and vigilance disorders - Thirst - Tracheo-esophageal fistula / esophageal atresia / stenosis