Disease #02015 (Rabson-Mendenhall syndrome, OMIM:262190)

Official abbreviation -
Name Rabson-Mendenhall syndrome
OMIM ID 262190
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene INSR
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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00080794 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - IMD28, Rabson-Mendenhall syndrome Immunodeficiency 28, mycobacteriosis (OMIM:614889), Rabson-Mendenhall syndrome (OMIM:262190) IFNGR2, INSR IFNGR2, INSR 2 1 Daniel Trujillano
00080809 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - Rabson-Mendenhall syndrome Rabson-Mendenhall syndrome (OMIM:262190) INSR INSR 1 1 Daniel Trujillano
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