Disease #01623 (IAD (ACTH deficiency, isolated (IAD)), OMIM:201400)

Official abbreviation IAD
Name ACTH deficiency, isolated (IAD)
OMIM ID 201400
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 4
Phenotype entries for this disease 2
Associated with 1 gene TBX19
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

4 entries on 1 page. Showing entries 1 - 4.
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00375265 179855 - - M ? Turkey - - - - - IAD Congenital ACTH deficiency, secondary adrenal insufficiency TBX19 TBX19 1 1 Andreas Laner
00428113 Fam3PatII3/4 PubMed: Charnay 2023, Journal: Charnay 2023 2-generation family, affected brother/sister, unaffected heterozygous carrier parentsneonatal F;M yes France Morocco >07y - - - IAD see paper; ... TBX19 TBX19 1 2 Alexandru SAVEANU
00460350 Fam1PatIv4 PubMed: Charnay 2023, Journal: Charnay 2023 4-generation family, 1 affected, unaffected heterozygous carrier parents M yes Morocco - - - - - IAD - TBX19 TBX19 1 1 Johan den Dunnen
00460351 Fam2PatIV1 PubMed: Charnay 2023, Journal: Charnay 2023 4-generation family, 1 affected, unaffected heterozygous carrier parents/relatives M - France Morocco - - - - IAD - TBX19 TBX19 1 1 Johan den Dunnen
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