del(21q22) disease
|
DIS: 51 |
|
Array
(
[MalformativeDisease] => Array
(
[id] => 51
[name] => del(21q22) disease
[description] => PMID: 21031080
[category_id] =>
[gene_id] =>
[chromosomal_anomaly_id] =>
[infectious_agent_id] =>
[toxic_agent_id] =>
[maternal_condition_id] =>
[omim_ref] =>
[humpath_ref] => 16577
[snomed_ref] =>
[adicap_ref] =>
[orphanet_ref] =>
[emedicine_ref] =>
[fetusnet_ref] =>
[possum_ref] =>
[ICD10_ref] =>
[diseasesdb_ref] =>
[mesh_ref] =>
[wiki_ref] =>
)
[Category] => Array
(
[id] =>
[name] =>
[description] =>
)
[InfectiousAgent] => Array
(
[id] =>
[name] =>
[description] =>
)
[ToxicAgent] => Array
(
[id] =>
[name] =>
[description] =>
)
[MaternalCondition] => Array
(
[id] =>
[name] =>
[description] =>
)
[Gene] => Array
(
[id] =>
[code] =>
[HUGO_code] =>
[protein_name] =>
[chromosomal_region_id] =>
[function_id] =>
[omim_ref] =>
[humpath_ref] =>
[gentests_ref] =>
[entrez_ref] =>
[uniprot_ref] =>
[ensembl_ref] =>
[orphanet_ref] =>
[mint_ref] =>
[gencard_ref] =>
)
[ChromosomalAnomaly] => Array
(
[id] =>
[abbreviation] =>
[name] =>
[chromosome_id] =>
[from_region] =>
[to_region] =>
[anomaly_id] =>
[category_id] =>
[humpath_ref] =>
)
[Diagnosis] => Array
(
)
[DiseaseSynonyms] => Array
(
)
[DAs] => Array
(
)
[SignalingPathways] => Array
(
)
)