Disease #00632 (ABS1 (Antley-Bixler syndrome, with genital anomalies and disordered steroidogenesis (ABS-1)), OMIM:201750)

Official abbreviation ABS1
Name Antley-Bixler syndrome, with genital anomalies and disordered steroidogenesis (ABS-1)
OMIM ID 201750
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene POR
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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00091783 - PubMed: Huang 2005 - - no Ireland - - - - - ABS1 see paper; ... FGFR1, FGFR2, POR FGFR1, POR 3 1 Johan den Dunnen
00091786 - PubMed: Huang 2005 - - no Australia Laotian, white - - - - ABS1 see paper; ... POR POR 2 1 Johan den Dunnen
00091788 - PubMed: Huang 2005 - - no - white, Moroccan - - - - ABS1 see paper; ... POR POR 2 1 Johan den Dunnen
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