Disease #01009 (IGHD2 (growth hormone deficiency, isolated, type II (IGHD-2)), OMIM:173100)

Official abbreviation IGHD2
Name growth hormone deficiency, isolated, type II (IGHD-2)
OMIM ID 173100
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene GH1
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

2 entries on 1 page. Showing entries 1 - 2.
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00132792 11836331-Fam PubMed: Moseley 2002 4-generation family, 5 affecteds (2F, 3M) F;M no Switzerland - - - - - IGHD2 see paper; ... GH1 GH1 1 5 Johan den Dunnen
00449782 - - - - - - - - - - - IGHD2 - GH1 GH1 1 1 Dan Feng Fang
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