Wikidata:Database reports/Constraint violations/P2841
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Constraint violations report for age of onset (Discussion, uses, items, changes, related properties): age group in which disease manifestations appear
Data time stamp: (UTC) — Items processed: 6
The report is generated based on the settings on Property:P2841#P2302.
Updates overwrite this page. Some may already be fixed since the last update: check RecentChangesLinked.
When incremental dumps and the bot work as planned, items fixed before 07:00 UTC disappear in the next update. The report is not updated if only the item count changes.
The report can include false positives. There is no need to "fix" them.
Data time stamp: (UTC) — Items processed: 6
The report is generated based on the settings on Property:P2841#P2302.
Updates overwrite this page. Some may already be fixed since the last update: check RecentChangesLinked.
When incremental dumps and the bot work as planned, items fixed before 07:00 UTC disappear in the next update. The report is not updated if only the item count changes.
The report can include false positives. There is no need to "fix" them.
"Type physiological condition (Q7189713)" violations[edit]
Violations count: 0
Types statistics[edit]
Accepted | Type | Usage |
---|---|---|
Yes | disease (Q12136) | 3 |
Yes | metabolic disease (Q2351083) | 1 |
Yes | pigmentation disorder (Q7193408) | 1 |
Yes | neonatal hyperbilirubinemia (Q68155417) | 1 |
Yes | carbohydrate metabolic disorder (Q6013981) | 1 |
Yes | genetic syndromic Pierre robin syndrome (Q55787783) | 1 |
Yes | rare syndrome with cardiac malformations (Q55785518) | 1 |
Yes | crystal arthropathy (Q5191403) | 1 |
Yes | central nervous system neoplasm (Q4335557) | 1 |
Yes | general symptom (Q31836626) | 1 |
Yes | genetic disease (Q200779) | 1 |
Yes | X-linked disease (Q18553438) | 1 |
Yes | syndrome (Q179630) | 1 |
Yes | food intolerance (Q1727229) | 1 |
Yes | arthritis (Q170990) | 1 |
Yes | malabsorption (Q1442923) | 1 |
Yes | jaundice (Q133244) | 1 |
"Value type age of a person (Q185836), developmental stage (Q48834911)" violations[edit]
Violations count: 0
Types statistics[edit]
Accepted | Type | Usage |
---|---|---|
Yes | age of onset (Q4691924) | 4 |
Yes | age of a person (Q185836) | 1 |
Yes | developmental stage (Q48834911) | 1 |
Yes | infancy stage (Q49257364) | 1 |
"Scope" violations[edit]
Violations count: 23
- post-traumatic stress disorder in children (Q97663028): subclass of (P279): post-traumatic stress disorder (Q202387)
- transient neonatal hyperparathyroidism (Q110916538): symptoms and signs (P780): aminoaciduria (Q4746440)
- transient neonatal hyperparathyroidism (Q110916538): symptoms and signs (P780): elevated alkaline phosphatase (Q17011974)
- transient neonatal hyperparathyroidism (Q110916538): symptoms and signs (P780): hepatomegaly (Q1362864)
- transient neonatal hyperparathyroidism (Q110916538): symptoms and signs (P780): hypotonia (Q1753547)
- transient neonatal hyperparathyroidism (Q110916538): symptoms and signs (P780): osteopenia (Q1367706)
- transient neonatal hyperparathyroidism (Q110916538): symptoms and signs (P780): polyhydramnios (Q976163)
- transient neonatal hyperparathyroidism (Q110916538): symptoms and signs (P780): respiratory distress (Q7315912)
- transient neonatal hyperparathyroidism (Q110916538): symptoms and signs (P780): short stature (Q7502090)
- transient neonatal hyperparathyroidism (Q110916538): symptoms and signs (P780): splenomegaly (Q1129121)
- transient neonatal hyperparathyroidism (Q110916538): symptoms and signs (P780): thin ribs (Q110916993)
- transient neonatal hyperparathyroidism (Q110916538): symptoms and signs (P780): feeding difficulties (Q110917143)
- transient neonatal hyperparathyroidism (Q110916538): symptoms and signs (P780): femoral bowing (Q110917167)
- transient neonatal hyperparathyroidism (Q110916538): symptoms and signs (P780): thyroid gland disease (Q6673122)
- transient neonatal hyperparathyroidism (Q110916538): symptoms and signs (P780): developmental language disorder (Q2313089)
- transient neonatal hyperparathyroidism (Q110916538): symptoms and signs (P780): motor delay (Q110917350)
- transient neonatal hyperparathyroidism (Q110916538): symptoms and signs (P780): narrow chest (Q110917364)
- transient neonatal hyperparathyroidism (Q110916538): symptoms and signs (P780): multiple fracture (Q55083281)
- transient neonatal hyperparathyroidism (Q110916538): symptoms and signs (P780): short ribs (Q110917449)
- transient neonatal hyperparathyroidism (Q110916538): symptoms and signs (P780): abnormal calcium-phosphate regulating hormone level (Q110917493)
- transient neonatal hyperparathyroidism (Q110916538): symptoms and signs (P780): abnormality of the metaphysis (Q110917535)
- glucocorticoid deficiency 2 (Q55999739): has phenotype (P6532): Decreased circulating cortisol level (Q110938301)
- glucocorticoid deficiency 2 (Q55999739): has phenotype (P6532): Abnormality of circulating adrenocorticotropin level (Q110938407)