Disease #01050 (WS2E (Waardenburg syndrome, type 2E, with/without neurologic involvement (WS2E)), OMIM:611584)

Official abbreviation WS2E
Name Waardenburg syndrome, type 2E, with/without neurologic involvement (WS2E)
OMIM ID 611584
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene SOX10
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00381527 - PubMed: Batissoco 2021 - M no Brazil - - - - - WS2E Profound sensorineural hearing loss, Blue hypoplastic irides, Vestibular and semicircular canals dysplasia (mainly lateral and posterior), poorly characterized vestibular aqueduct. SOX10 SOX10 1 2 Karina Lezirovitz Mandelbaum
00381528 - PubMed: Batissoco 2021 - F no Brazil - - - - - WS2E iris heterochromia, white hair forelock and unilateral hearing loss SOX10 SOX10 1 1 Karina Lezirovitz Mandelbaum
00416319 - - - M no China - - - - - WS2E - SOX10 SOX10 1 1 Ke Xu
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