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CRRD ID: 3461
Species: Rattus norvegicus
CRRD Object: Gene
Symbol: Pygm
Name: glycogen phosphorylase, muscle associated
Acc ID: DOID:630
Term: genetic disease
Definition: Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero.
Definition Source(s): MESH:D030342,
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
QualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
 ISORGD:7373298554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases

PMID:1067063, PMID:11168025, PMID:11706962, PMID:12223025, PMID:12666117, PMID:14748827, PMID:16786513, PMID:16924035, PMID:17221871, PMID:17324573, PMID:17404776, PMID:17630210, PMID:17915571, PMID:17994553, PMID:20301518, PMID:21802952, PMID:22250184, PMID:22730558, PMID:23653251, PMID:2391551, PMID:24033266, PMID:25240406, PMID:25740218, PMID:25741868, PMID:25873271, PMID:25914343, PMID:28492532, PMID:3458722, PMID:3466902, PMID:3476861, PMID:4513544, PMID:8316268, PMID:8401511, PMID:9131647, PMID:9506549, PMID:9674815
 ISORGD:7373298554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases

PMID:12223025, PMID:12666117, PMID:16924035, PMID:17630210, PMID:17915571, PMID:17994553, PMID:25741868, PMID:25914343, PMID:3458722, PMID:3466902, PMID:4513544, PMID:8316268
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.