Disease #00904 (ALSG (aplasia of lacrimal and salivary glands (ALSG)), OMIM:180920)

Official abbreviation ALSG
Name aplasia of lacrimal and salivary glands (ALSG)
OMIM ID 180920
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 5
Phenotype entries for this disease 5
Associated with 1 gene FGF10
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-02-22 10:25:31 +01:00 (CET)


Individuals

5 entries on 1 page. Showing entries 1 - 5.
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00332558 Fam1 PubMed: Entesarian 2005 4-generation family, 12 affected (6F, 6M) F;M no Sweden - - - - - ALSG see paper; ..., irritable eyes, dryness mouth FGF10 FGF10 1 12 Johan den Dunnen
00332559 Fam2 PubMed: Entesarian 2005 3-generation family, 4 qffected (2F, 2M) F;M - Sweden - - - - - ALSG see paper; ..., irritable eyes, dryness mouth FGF10 FGF10 1 4 Johan den Dunnen
00332568 Fam2 PubMed: Milunksy 2006 2-generation family, affected, mother/daughter F no United States - - - - - ALSG see paper; ... FGF10 FGF10 1 2 Johan den Dunnen
00332569 Fam1 PubMed: Entesarian 2007 2-generation family, affected fahter/son M - - white - - - - ALSG see paper; ... FGF10 FGF10 2 2 Johan den Dunnen
00332570 Fam2 PubMed: Entesarian 2007 2-generation family, 1 affected, unaffected heterozygous carrier parents M - United States - - - - - ALSG see paper; ... FGF10 FGF10 1 1 Johan den Dunnen
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