Disease #01727 (TEMTYS (Temtamy syndrome), OMIM:218340)

Official abbreviation TEMTYS
Name Temtamy syndrome
OMIM ID 218340
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 5
Phenotype entries for this disease 5
Associated with 1 gene C12orf57
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

5 entries on 1 page. Showing entries 1 - 5.
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00080825 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - TEMTYS Temtamy syndrome (OMIM:218340) C12orf57 C12orf57 1 1 Daniel Trujillano
00080849 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - TEMTYS Temtamy syndrome (OMIM:218340) C12orf57 C12orf57 1 1 Daniel Trujillano
00080876 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - TEMTYS Temtamy syndrome (OMIM:218340) C12orf57 C12orf57 1 1 Daniel Trujillano
00080881 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - TEMTYS Temtamy syndrome (OMIM:218340) C12orf57 C12orf57 1 1 Daniel Trujillano
00080948 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - TEMTYS Temtamy syndrome (OMIM:218340) C12orf57 C12orf57 1 1 Daniel Trujillano
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