Disease #01403 (KIDAD (keratitis-ichthyosis-deafness syndrome, autosomal dominant), OMIM:148210)

Official abbreviation KIDAD
Name keratitis-ichthyosis-deafness syndrome, autosomal dominant
OMIM ID 148210
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 GJB2
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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00081072 - PubMed: Trujillano 2017 unaffected non-carrier parents - - - - - - - - KIDAD Keratitis-ichthyosis-deafness syndrome (OMIM:148210) GJB2 GJB2 1 1 Daniel Trujillano
00428699 Pat1 PubMed: Wonkam 2013 2-generation family, 1 affected, unaffected parents F - Cameroon Africa >05y - - - KIDAD Keratoderma of the soles (HP:0000982), chronic otitis externa (HP:0000389), Hypohidrosis (HP:0000966), normal psychomotor development (-HP:0001263), Thickened skin (HP:0001072), Xeroderma pigmentosum (ORPHA:910), aged facial appearance (HP:0005328), hypotrichosis (HP:0008070), Hyperkeratosis (HP:0000962), Photophobia (HP:0000613), Reduced visual acuity (HP:0007663), Dental dysplasia, Epidermal acanthosis (HP:0025092) GJB2 GJB2 1 1 Yacouba Dia
00428700 Pat2 PubMed: Wonkam 2013 2-generation family, 1 affected, unaffected parents F no Cameroon Africa >02y - - - KIDAD Thickened skin (HP:0001072), Dry skin HP:0000958, Ichthyosis HP:0008064, Alopecia HP:0001596, absent eyelashes HP:0200102, Aplasia of the eyebrow HP:0100840, Photophobia HP:0000613, GJB2 GJB2 1 1 Yacouba Dia
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