Disease #03002 (PSATD (deficiency, phosphoserine aminotransferase (PSATD)), OMIM:610992)

Official abbreviation PSATD
Name deficiency, phosphoserine aminotransferase (PSATD)
OMIM ID 610992
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene PSAT1
Associated tissues -
Disease features -
Remarks -


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00300229 - - - M yes Turkey - >04y 0 - - PSATD HP:0001511, HP:0000340, HP:0000470, HP:0000377, HP:0000369, HP:0000153, HP:0000232, HP:0009099, HP:0000278, HP:0000537, HP:0002057, HP:0000520, HP:0007651, HP:0000518, HP:0000252, HP:0002079, HP:0001371, HP:0001838, HP:0001188 PSAT1 PSAT1 1 1 Fatima Abdelfattah
00300230 - - - M yes Turkey - 06y06m00d00h - - - PSATD HP:0001511, HP:0000340, HP:0000470, HP:0000377, HP:0000175, HP:0000347, HP:0000537, HP:0000520, HP:0000518, HP:0000252, HP:0001371, HP:0001188 PSAT1 PSAT1 1 1 Fatima Abdelfattah
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