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Waardenburg syndrome type 2

5 OMIM references -
3 associated genes
13 signs/symptoms

PROTEIN INTERACTIONS: 1

Parietal foramina

3 OMIM references -
2 associated genes
No signs/symptoms info

Waardenburg syndrome type 2

Parietal foramina

MITF	(UniProt - OMIM)		ALX4	(UniProt - OMIM)
SNAI2	(UniProt - OMIM)		MSX2	(UniProt - OMIM)
SOX10	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SOX10	(0.63)	ALX4

Citations in the biomedical literature:

Waardenburg syndrome type 2		Parietal foramina
	Synonym(s): (no synonyms)		Synonym(s): - Catlin marks - Enlarged parietal foramina - Foramina parietalia permagna - Hereditary cranium bifidum

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic disease - Rare maxillo-facial surgical disease - Rare otorhinolaryngologic disease - Rare skin disease		Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant

	External references: 5 OMIM references - 1 MeSH reference: C536463		External references: 3 OMIM references - No MeSH references

Waardenburg syndrome type 2
	Very frequent - Autosomal dominant inheritance - Decreased hair pigmentation / hypopigmentation of hair - Hearing loss / hypoacusia / deafness - Heterochromia / mixed colouring of iris - Premature greying of hair - Sensorineural deafness / hearing loss Frequent - Irregular / patchy skin hypopigmentation - White forelock / piebaldism Occasional - Dolichocolon / megacolon / megadolichocolon / Hirschsprung's disease - Ptosis - Pulmonary artery stenosis / absence / hypoplasia of the pulmonary branches - Renal / kidney anomalies - Telecanthus / canthal dystopy
Parietal foramina
(no data available)