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5 OMIM references -
3 associated genes
13 signs/symptoms
PROTEIN INTERACTIONS: 2
COMMON SIGNS: 1
1 OMIM reference -
1 associated gene
3 signs/symptoms
Waardenburg syndrome type 2
Hereditary cerebral hemorrhage with amyloidosis, Arctic type

MITF APP
SNAI2
SOX10


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
MITF
SNAI2
(0.56)
(0.56)
APP
APP



Citations in the biomedical literature:


Waardenburg syndrome type 2
MITF SNAI2 SOX10
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
APP



Waardenburg syndrome type 2
Hereditary cerebral hemorrhage with amyloidosis, Arctic type

Synonym(s):
(no synonyms)

Synonym(s):
- HCHWA, Arctic type

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 genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
(no data available)

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:
1 OMIM reference -
No MeSH references


COMMON
SIGNS
- Autosomal dominant inheritance


Waardenburg syndrome type 2
Hereditary cerebral hemorrhage with amyloidosis, Arctic type

Very frequent
- 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


Very frequent
- Psychic / behavioural troubles
- Psychic / psychomotor regression / dementia / intellectual decline