Preferred Name |
Imprinting Disorders |
|
Synonyms |
Genetic Imprinting Disorders Syndrome, Imprinting Imprinting Disorder Disorder, Imprinting Imprinting Disorder, Genetic Imprinting Syndromes Disorder, Genomic Imprinting Imprinting Disorder, Genomic Genetic Imprinting Disorder Disease, Imprinting Genomic Imprinting Disorder Disorder, Genetic Imprinting Imprinting Disease Imprinting Syndrome Imprinting Diseases Genomic Imprinting Disorders |
|
Definitions |
Disorders caused by transcriptional silencing of one parental gene allele (imprinted gene). Imprinted genes show genetic expression from only one parent of the gene pair through epigenetic processes with no change in the DNA sequence. |
|
ID |
http://purl.bioontology.org/ontology/MESH/D000096803 |
|
altLabel |
Genetic Imprinting Disorders Syndrome, Imprinting Imprinting Disorder Disorder, Imprinting Imprinting Disorder, Genetic Imprinting Syndromes Disorder, Genomic Imprinting Imprinting Disorder, Genomic Genetic Imprinting Disorder Disease, Imprinting Genomic Imprinting Disorder Disorder, Genetic Imprinting Imprinting Disease Imprinting Syndrome Imprinting Diseases Genomic Imprinting Disorders |
|
AQL |
BL CF CI CL CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI |
|
cui |
C5816793 |
|
DC |
1 |
|
definition |
Disorders caused by transcriptional silencing of one parental gene allele (imprinted gene). Imprinted genes show genetic expression from only one parent of the gene pair through epigenetic processes with no change in the DNA sequence. |
|
DX |
20240101 |
|
HN |
2024 |
|
Inverse of AQ |
http://purl.bioontology.org/ontology/MESH/Q000097 http://purl.bioontology.org/ontology/MESH/Q000178 http://purl.bioontology.org/ontology/MESH/Q000175 http://purl.bioontology.org/ontology/MESH/Q000628 http://purl.bioontology.org/ontology/MESH/Q000276 http://purl.bioontology.org/ontology/MESH/Q000134 http://purl.bioontology.org/ontology/MESH/Q000139 http://purl.bioontology.org/ontology/MESH/Q000266 http://purl.bioontology.org/ontology/MESH/Q000378 http://purl.bioontology.org/ontology/MESH/Q000517 http://purl.bioontology.org/ontology/MESH/Q000662 http://purl.bioontology.org/ontology/MESH/Q000469 http://purl.bioontology.org/ontology/MESH/Q000150 http://purl.bioontology.org/ontology/MESH/Q000821 http://purl.bioontology.org/ontology/MESH/Q000191 http://purl.bioontology.org/ontology/MESH/Q000196 http://purl.bioontology.org/ontology/MESH/Q000473 http://purl.bioontology.org/ontology/MESH/Q000145 http://purl.bioontology.org/ontology/MESH/Q000382 http://purl.bioontology.org/ontology/MESH/Q000451 http://purl.bioontology.org/ontology/MESH/Q000453 http://purl.bioontology.org/ontology/MESH/Q000534 http://purl.bioontology.org/ontology/MESH/Q000532 http://purl.bioontology.org/ontology/MESH/Q000503 http://purl.bioontology.org/ontology/MESH/Q000188 http://purl.bioontology.org/ontology/MESH/Q000235 http://purl.bioontology.org/ontology/MESH/Q000201 http://purl.bioontology.org/ontology/MESH/Q000209 http://purl.bioontology.org/ontology/MESH/Q000208 http://purl.bioontology.org/ontology/MESH/Q000601 http://purl.bioontology.org/ontology/MESH/Q000000981 http://purl.bioontology.org/ontology/MESH/Q000652 |
|
Machine permutation |
2024 |
|
Mapped from |
http://purl.bioontology.org/ontology/MESH/C579872 http://purl.bioontology.org/ontology/MESH/C000726750 |
|
MDA |
20230726 |
|
MMR |
20230601 |
|
MN |
C16.320.447 |
|
notation |
D000096803 |
|
prefLabel |
Imprinting Disorders |
|
TERMUI |
T001132682 T001132680 T001132679 T001132681 T001132678 |
|
TH |
NLM (2024) |
|
tui |
T047 |
|
subClassOf |
Delete | Mapping To | Ontology | Source |
---|---|---|---|
http://www.orpha.net/ORDO/Orphanet_641343 | ORDO | LOOM |