sameAs
Dyschromatosis universalis hereditaria: evidence for autosomal recessive inheritance and identification of a new locus on chromosome 12q21-q23Mutations in ABCB6 cause dyschromatosis universalis hereditariaThrombocytopenia in dyschromatosis universalis hereditaria.Dyschromatosis universalis hereditaria: report of a case and review of the literature.Novel mutations of ABCB6 associated with autosomal dominant dyschromatosis universalis hereditaria.Photoletter to the editor: Dyschromatosis universalis hereditaria: an infrequently occurring entity in EuropeA Case Report of Dyschromatosis Universalis Hereditaria (DUH) with Primary Ovarian Failure (POF).Dyschromatosis universalis hereditaria: Infrequent genodermatoses in India.Genome-wide linkage, exome sequencing and functional analyses identify ABCB6 as the pathogenic gene of dyschromatosis universalis hereditaria.Dyschromatosis Universalis Hereditaria with Oral Leukokeratosis--A Case of Mistaken Identity and Review of the Literature.Dyschromatosis universalis hereditaria: two cases.Dyschromatosis universalis hereditaria with renal failureDyschromatosis universalis hereditaria with involvement of palms.A Case of Sporadic Dyschromatosis Universalis Hereditaria.Dyschromatosis universalis hereditaria: report of a case.A case of dyschromatosis universalis hereditaria with adermatoglyphia: A rare association.Dyschromatosis universalis hereditaria in an African American male.Mutation analysis of the ADAR1 gene in dyschromatosis symmetrica hereditaria and genetic differentiation from both dyschromatosis universalis hereditaria and acropigmentatio reticularis.Removal of facial and labial lentigines in dyschromatosis universalis hereditaria with a Q-switched alexandrite laser.Removal of forearm lentigines in dyschromatosis universalis hereditaria with a 755-nm Q-switched alexandrite laser.Dyschromatosis universalis hereditaria in a young Nigerian female.Dyschromatosis universalis hereditaria: a rare entity.Dyschromatosis universalis hereditaria: familial case and ultrastructural skin investigation.Ultrastructural Investigations in an Autosomal Recessively Inherited Case of Dyschromatosis Universalis Hereditaria.Dyschromatosis universalis hereditaria: a case report.Dyschromatosis universalis hereditariaDyschromatosis Universalis Hereditaria: A Unique Disorder
P921
Q28279259-36F4BA8D-4D78-4308-8A12-1B0C47D19AE4Q28594264-29983F13-C0B5-48AE-81FC-B3733BB674D7Q33403941-47A9127F-8C3F-49B2-BDE1-36A706ED90BCQ35001095-78EEA62A-8A1D-4B41-A85A-2E3DD1431B10Q35041502-7433FE26-BE2D-4984-9D42-4D0FE746682AQ36315642-7B87F67D-2038-46D1-A434-B3E76A89EF71Q36831328-C8B6DEB6-3619-455B-9E87-AF9E0EE96125Q37498473-53EEA1E7-4794-4E62-91A8-B3F25EC83EDBQ37548448-CFF8E7E4-5E63-49BC-9D2C-FCF3D3533BECQ38565730-19FA5E5D-02F3-47BF-87DE-87F4CD823CE0Q39128006-E79A224C-5CE3-4D7C-83BF-71D1E61E3FC1Q40528308-2EE8B286-F297-4B71-8D0E-2362D32101EAQ41836757-B980C82C-A2B0-4FB2-8FA5-DD1328235BC7Q42073670-35FA15D4-C9A2-4B2C-AEAD-49AC1F6BF618Q42465074-E600F6FF-BDD1-4A6E-A739-CBAAAB228D75Q42684869-924A8956-B873-40F2-9348-6D45ABF0648EQ46304313-AB92BC48-0DF9-4FA6-BA85-B3DCB44CC7E2Q46545773-0628E4B3-4D48-4907-9C60-9897EE12B69BQ48629048-E2D2F0C7-A09D-409B-AE42-4728F4A0B03BQ49200446-26A3EF4E-6CF4-496A-9A8E-7A8E29694A02Q50609294-A23E80EB-55E6-43BF-B8DC-1A7502BE4BDDQ51430820-A2565FD8-A536-45FE-9A69-C254798B90CDQ52946457-9554DA49-E557-4019-8938-235A4DA1D207Q53676949-8AACB82A-4854-4CE1-AEF3-D177BDBA2137Q53794872-CBDA23C7-0A81-40E7-ACA8-5C3420187722Q58623537-1B43C632-95DC-4323-BBA7-F4104145D71DQ58623593-46154590-6618-4632-AB97-DD9BF0F6B18B
P921
description
Krankheit
@de
maladie
@fr
pigmentation disease character ...... in a generalized distribution
@en
name
dyschromatose universelle héréditaire
@fr
dyschromatosis universalis hereditaria
@en
type
label
dyschromatose universelle héréditaire
@fr
dyschromatosis universalis hereditaria
@en
altLabel
DUH
@en
DUH1
@en
DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 1
@en
dyschromatosis universalis
@en
prefLabel
dyschromatose universelle héréditaire
@fr
dyschromatosis universalis hereditaria
@en
P1550
P2888
P2892
P492
P486
P6366
P2293
P2892
P4229
P486
P492
P5270
MONDO:0000736
MONDO:0007484
P6366
2775982734
P699
DOID:0060304