porphyria cutanea tardaerythropoietic protoporphyriaHuntington diseaseautosomal dominant sideroblastic anemiachromosome 1q21.1 deletion syndromedistal 10q deletion syndromechromosome 15q13.3 microdeletion syndromechromosome 17q12 deletion syndromechromosome 16p11.2 duplication syndromechromosome 17q12 duplication syndromeJob's syndromechromosome 1q21.1 duplication syndromeautosomal dominant polycystic kidneyvariegate porphyriaphotomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunctionacryocystitis-osteopoikilosis syndromeauriculo condylar syndromeD,L-2-hydroxyglutaric aciduriaacute intermittent porphyriaautosomal dominant cutis laxaFlynn–Aird syndromepure or complex autosomal dominant spastic paraplegiaautosomal dominant keratitiscardiac malformation, cleft lip/palate, microcephaly, and digital anomaliesautosomal dominant distal myopathyautosomal dominant proximal spinal muscular atrophyautosomal dominant Wolfram syndromeneurofibromatosis type Ihereditary hemorrhagic telangiectasiaVohwinkel syndrome
P1199
Familial Cleidocranial Dysplasia.Congenital central hypoventilation syndrome: Severe disease caused by co-occurrence of two PHOX2B variants inherited separately from asymptomatic family membersParathyroid Carcinoma Causing Mild Hyperparathyroidism in Neurofibromatosis Type 1: A Case Report and Systematic ReviewNovel EYA4 variant in Slovak family with late onset autosomal dominant hearing loss: a case report
P921
Q1479497-135107dd-466c-9a0a-72d6-4c248f86e0cfQ1759600-a5c4bd41-453e-fb77-3e5f-7bdec592cc13Q190564-54543797-4a3d-2c52-9505-c03e317114abQ19833018-01772d9c-4cbd-df3b-217f-8f6db435acf6Q209049-AE331F0A-B969-416F-BF73-52B553145015Q21154055-A0F9213C-D0E3-468A-9BA3-5EF89832AB2BQ21154058-841E1F66-8E90-40A4-8F7E-85E5E2CDE611Q21154064-7CBF5ADD-F392-4185-B8ED-12CAD0275CCBQ21154076-1E2048A5-7718-4D25-81F0-62F0C604B99EQ21154079-41B93898-9BB7-47BC-ADB4-56A7C681993DQ2336873-e2b2d764-463d-ec70-17d1-dc6c6a85df39Q2692054-E9031CD7-024F-4285-8D4D-742D502F550DQ2732398-625b604e-4643-709d-bfb7-d7a032cc1e64Q275385-396084fe-47d6-7f7d-39ed-75240e04237cQ29014962-C872365B-E4EB-49AB-B302-9656BB9AE245Q29014964-E3D2E72D-55B2-4A75-8AE3-08774CF5D278Q29014971-79264496-B6BC-45C1-A461-0096ACED8BCDQ29982079-A2BCDAAB-DED0-4170-99EA-4E24A54652C1Q424247-694598d1-43c6-968d-5f61-285ab7a79084Q50349708-36fcf160-40b0-9abe-2f45-323c111436c8Q5463653-0644b45b-4b7a-427e-ed16-91f278ca4b27Q55346013-7e86a940-414f-1df2-a5ff-1de635d71aa7Q55781158-8e56e461-4dc8-06a1-9bd6-ed95a97251b7Q55782890-a22a1f6e-42c4-539c-d773-cf34f8143ab2Q55785936-89adba38-4064-4ff8-c1dd-20e6b833ca9aQ55786069-d90c0c42-4bbf-8785-a655-45109ea8c398Q66804102-3ca87b5d-481b-ed0d-c6e1-97ef1d5598ddQ7616509-4444c56b-4b90-81eb-8905-aea2ac509a10Q776881-c827463a-40f7-f707-5445-d73d2daff645Q7939442-C085ABE2-664D-4041-8FA2-257B47EF5A7B
P1199
description
Caractéristique médicale propre à la transmission des maladies génétiques
@fr
mode of inheritance
@en
način nasljeđivanja
@hr
характер наследования признака
@ru
ժառանգման տարբերակ
@hy
name
Autosomal dominant
@nb
Autosomal-dominanter Erbgang
@de
Dziedziczenie autosomalne dominujące
@pl
Trashëgimia autosomale
@sq
autosomal dominant
@en
autosomalt dominant
@nn
autosomno dominantno
@hr
aŭtosoma dominado
@eo
transmisión autosómica dominante
@es
transmission autosomique dominante
@fr
type
label
Autosomal dominant
@nb
Autosomal-dominanter Erbgang
@de
Dziedziczenie autosomalne dominujące
@pl
Trashëgimia autosomale
@sq
autosomal dominant
@en
autosomalt dominant
@nn
autosomno dominantno
@hr
aŭtosoma dominado
@eo
transmisión autosómica dominante
@es
transmission autosomique dominante
@fr
altLabel
AD
@en
AD
@hr
Autosomal dominant form
@en
Autosomal dominant type
@en
Autosomal dominant
@en
Gen autosomalny dominujący
@pl
automosmno dominantno nasljeđivanje
@hr
autosomal dominans
@nn
autosomal dominant inheritance
@en
autosomalt dominant arv
@nn
prefLabel
Autosomal dominant
@nb
Autosomal-dominanter Erbgang
@de
Dziedziczenie autosomalne dominujące
@pl
Trashëgimia autosomale
@sq
autosomal dominant
@en
autosomalt dominant
@nn
autosomno dominantno
@hr
aŭtosoma dominado
@eo
transmisión autosómica dominante
@es
transmission autosomique dominante
@fr
P2888
P2892
P3841
HP:0000006