Monosomy X disease
|
DIS: 4 |
|
Array
(
[MalformativeDisease] => Array
(
[id] => 4
[name] => Monosomy X disease
[description] => Turner syndrome is a genetic disorder that affects a girl’s development. The cause is a missing or incomplete X chromosome.
[category_id] => 1
[gene_id] =>
[chromosomal_anomaly_id] =>
[infectious_agent_id] =>
[toxic_agent_id] =>
[maternal_condition_id] =>
[omim_ref] =>
[humpath_ref] => 5349
[snomed_ref] =>
[adicap_ref] =>
[orphanet_ref] =>
[emedicine_ref] =>
[fetusnet_ref] =>
[possum_ref] =>
[ICD10_ref] =>
[diseasesdb_ref] =>
[mesh_ref] =>
[wiki_ref] =>
)
[Category] => Array
(
[id] => 1
[name] => Chromosomal disease
[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
(
[0] => Array
(
[id] => 66
[case_id] => 42
[isolated_da_id] => 0
[sequence_id] => 0
[syndrome_id] => 0
[disease_id] => 4
[is_isolated] => 0
[is_known] => 1
)
[1] => Array
(
[id] => 126
[case_id] => 102
[isolated_da_id] => 0
[sequence_id] => 0
[syndrome_id] => 0
[disease_id] => 4
[is_isolated] => 0
[is_known] => 1
)
)
[DiseaseSynonyms] => Array
(
[0] => Array
(
[id] => 1
[disease_id] => 4
[name] => Turner syndrome
)
)
[DAs] => Array
(
)
[SignalingPathways] => Array
(
)
[Cases] => Array
(
[0] =>
[1] =>
)
)