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2 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
5 OMIM references -
3 associated genes
13 signs/symptoms
Autosomal dominant secondary polycythemia
Waardenburg syndrome type 2

EGLN1 MITF
EPAS1 SNAI2
SOX10


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
EPAS1
EPAS1
(0.63)
(0.63)
MITF
SOX10



Citations in the biomedical literature:


Autosomal dominant secondary polycythemia
EGLN1 EPAS1
Waardenburg syndrome type 2
MITF SNAI2 SOX10



Autosomal dominant secondary polycythemia
Waardenburg syndrome type 2

Synonym(s):
- Autosomal dominant secondary erythrocytosis

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
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 (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -

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

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

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


Autosomal dominant secondary polycythemia

(no data available)