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Waardenburg syndrome type 2

5 OMIM references -
3 associated genes
13 signs/symptoms

COMMON GENES: 1

Papillary renal cell carcinoma

1 associated gene
No signs/symptoms info

Waardenburg syndrome type 2

Papillary renal cell carcinoma

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


COMMON GENES	MITF

Citations in the biomedical literature:

Waardenburg syndrome type 2		Papillary renal cell carcinoma
	Synonym(s): (no synonyms)		Synonym(s): - Papillary renal cell adenocarcinoma

	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 oncologic disease - Rare renal disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Neoplasms -

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

	External references: 5 OMIM references - 1 MeSH reference: C536463		External references: No 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
Papillary renal cell carcinoma
(no data available)