Disease #01727

Official abbreviation -
Name Temtamy syndrome
OMIM ID 218340
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 5
Phenotype entries for this disease 5
Associated with 1 gene C12orf57
Associated tissues -
Disease features -
Remarks -


Individuals

5 entries on 1 page. Showing entries 1 - 5.
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00080825 - Trujillano et al., submitted unaffected parents - - - - - 0 - - Temtamy syndrome Temtamy syndrome (OMIM:218340) C12orf57 C12orf57 1 1 Daniel Trujillano
00080849 - Trujillano et al., submitted unaffected parents - - - - - 0 - - Temtamy syndrome Temtamy syndrome (OMIM:218340) C12orf57 C12orf57 1 1 Daniel Trujillano
00080876 - Trujillano et al., submitted unaffected parents - - - - - 0 - - Temtamy syndrome Temtamy syndrome (OMIM:218340) C12orf57 C12orf57 1 1 Daniel Trujillano
00080881 - Trujillano et al., submitted unaffected parents - - - - - 0 - - Temtamy syndrome Temtamy syndrome (OMIM:218340) C12orf57 C12orf57 1 1 Daniel Trujillano
00080948 - Trujillano et al., submitted unaffected parents - - - - - 0 - - Temtamy syndrome Temtamy syndrome (OMIM:218340) C12orf57 C12orf57 1 1 Daniel Trujillano
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