Wikidata:Database reports/Constraint violations/P668

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Constraint violations report for GeneReviews ID (Discussion, uses, items, changes, related properties): collection of peer-reviewed articles that describe specific gene-releated diseases
Data time stamp: (UTC) — Items processed: 151
The report is generated based on the settings on Property:P668#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.

"Format" violations

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Violations count: 1

"Type physiological condition (Q7189713)" violations

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Violations count: 0

Types statistics

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Accepted Type Usage
Yes disease (Q12136) 77
Yes syndrome (Q179630) 23
Yes autosomal dominant disease (Q18553439) 18
Yes autosomal recessive disease (Q10267817) 15
Yes genetic disease (Q200779) 11
Yes nervous system heredodegenerative disease (Q19001236) 8
Yes X-linked recessive disease (Q55010090) 7
Yes rare genetic developmental defect during embryogenesis (Q55785846) 7
Yes muscular dystrophy (Q1137767) 6
Yes neurometabolic disease (Q1337418) 6
Yes eye degenerative disease (Q18558225) 5
Yes leukodystrophy (Q1821559) 4
Yes syndromic developmental defect of the eye (Q55785336) 4
Yes periodic paralysis (Q1788314) 4
Yes autosomal genetic disease (Q18553442) 4
Yes genetic syndromic intellectual disability (Q55785866) 4
Yes osteochondrodysplasia (Q3251367) 4
Yes glycogen storage disease (Q1421738) 4
Yes neuroacanthocytosis (Q746781) 3
Yes ptosis (Q622427) 3
Yes metabolic disease with cataract (Q55789275) 3
Yes inherited renal tumor (Q55785849) 3
Yes metabolic disease with corneal opacity (Q55789274) 3
Yes amino acid metabolic disorder (Q18558086) 3
Yes lysosomal storage disease with skeletal involvement (Q55788818) 3
Yes organic brain syndrome (Q360341) 3
Yes chromosomal disease (Q4501577) 3
Yes rare metabolic liver disease (Q55785261) 3
Yes malformation syndrome with skin/mucosae involvement (Q55785402) 3
Yes syndrome associated with hypertrophic cardiomyopathy (Q55786146) 3
Yes polymalformative genetic syndrome with increased risk of developing cancer (Q55785832) 3
Yes rare genetic epilepsy (Q55785842) 3
Yes X-linked intellectual disability (Q8041560) 3
Yes hypertrophic cardiomyopathy (Q1364270) 3
Yes ectodermal dysplasia (Q1323713) 3
Yes mitochondrial disease with peripheral neuropathy (Q55786198) 2
Yes malformation syndrome with short stature (Q55785400) 2
Yes developmental anomaly of metabolic origin (Q55785399) 2
Yes hereditary retinal dystrophy (Q18557955) 2
Yes mitochondrial disease with eye involvement (Q55789259) 2
Yes multiple congenital anomalies/dysmorphic syndrome without intellectual disability (Q55785290) 2
Yes multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome (Q55785289) 2
Yes multiple congenital anomalies/dysmorphic syndrome-intellectual disability (Q55785288) 2
Yes mitochondrial disease with epilepsy (Q55786197) 2
Yes mucolipidosis (Q1952032) 2
Yes neurofibromatoses (Q847605) 2
Yes liver disease (Q929737) 2
Yes genetic cardiac rhythm disease (Q55785258) 2
Yes muscular channelopathy (Q55788493) 2
Yes genetic neurodegenerative disease with dementia (Q55346116) 2
Yes other metabolic disease with epilepsy (Q55786201) 2
Yes syndromic glaucoma (Q55789219) 2
Yes syndromic obesity (Q55786310) 2
Yes movement disorders (Q2608695) 2
Yes malformation syndrome with hamartosis (Q55789095) 2
Yes nephropathy secondary to a storage or other metabolic disease (Q55788855) 2
Yes syndromic microphthalmia (Q29982037) 2
Yes eye disease (Q3041498) 2
Yes intestinal disease (Q3055380) 2
Yes syndromic genetic deafness (Q55788734) 2
Yes androgen insensitivity syndrome (Q512313) 2
Yes neurological disorder (Q3339235) 2
Yes amino acid transport disorder (Q471778) 2
Yes catecholamine-producing tumor (Q55788491) 2
Yes mucopolysaccharidosis (Q1479681) 2
Yes progressive muscular dystrophy (Q55785935) 2
Yes marfanoid (Q6759035) 2
Yes kidney disease (Q1054718) 2
Yes syndromic neurometabolic disease with X-linked intellectual disability (Q55785814) 2
Yes muscular glycogenosis (Q55785945) 2
Yes lysosomal disease with hypertrophic cardiomyopathy (Q55786143) 2
Yes Primary lymphedema (Q7243149) 2
Yes long QT syndrome (Q653924) 2
Yes chromosomal deletion syndrome (Q16918398) 2
Yes mitochondrial disease with dilated cardiomyopathy (Q55786150) 2
Yes genetic hematologic disease (Q55785542) 2
Yes congenital structural myopathy (Q18556238) 2
Yes encephalopathy (Q576349) 2
Yes nervous system malformations (Q584265) 2
Yes progeroid syndrome (Q6139748) 2
Yes hyaline fibromatosis syndrome (Q102294089) 1
Yes rare genetic tremor disorder (Q55787262) 1
Yes lysosomal glycogen storage disease (Q55787314) 1
Yes rare genetic immune disease (Q55785867) 1
Yes mitochondrial disease (Q935710) 1
Yes peripheral neuropathy (Q945238) 1
Yes constitutional neutropenia with extra-hematopoietic manifestations (Q55787695) 1
Yes skin disease (Q949302) 1
Yes primary bone dysplasia (Q55787804) 1
Yes other genetic dermis disorder (Q55788349) 1
Yes rare disorder with dystonia and other neurologic or systemic manifestation (Q55787834) 1
Yes central nervous system and retinal vascular disease (Q55788489) 1
Yes rare genetic dystonia (Q55787960) 1
Yes rare disease with malignant hyperthermia (Q55788310) 1
Yes hereditary eye tumor (Q55785853) 1
Yes primary lymphedema with associated anomalies (Q55788282) 1
Yes rare bone disease (Q55788795) 1
Yes lymphedema (Q916398) 1
Yes genetic vascular anomaly (Q55786073) 1
Yes hereditary poikiloderma (Q55786182) 1
Yes lysosomal disease with epilepsy (Q55786192) 1
Yes rare disease (Q929833) 1
Yes lysosomal disease with restrictive cardiomyopathy (Q55786156) 1
Yes metal transport or utilization disorder with epilepsy (Q55786195) 1
Yes syndrome associated with dilated cardiomyopathy (Q55786153) 1
Yes osteomyelitis (Q938983) 1
Yes mitochondrial disease with hypertrophic cardiomyopathy (Q55786144) 1
Yes glycogen storage disease with hypertrophic cardiomyopathy (Q55786141) 1
Yes autoinflammatory syndrome with skin involvement (Q55787013) 1
Yes non-dystrophic myopathy (Q55785938) 1
Yes inherited nervous system cancer-predisposing syndrome (Q55786407) 1
Yes mitochondrial oxidative phosphorylation disorder due to a large-scale single deletion of mitochondrial DNA (Q55786429) 1
Yes mitochondrial oxidative phosphorylation disorder due to a point mutation of mitochondrial DNA (Q55786430) 1
Yes alpha-thalassemia and related diseases (Q55786861) 1
Yes rare disease with thoracic aortic aneurysm and aortic dissection (Q55786976) 1
Yes epidermolysis bullosa (Q923020) 1
Yes congenital heart disease (Q939364) 1
Yes disorder of lysine and hydroxylysine metabolism (Q55787002) 1
Yes hereditary spastic paraplegia (Q657516) 1
Yes myopathy with eye involvement (Q55789252) 1
Yes nervous system anomaly with eye involvement (Q55789255) 1
Yes dementia (Q83030) 1
Yes connective tissue disease with eye involvement (Q55789267) 1
Yes ectodermal malformation syndrome associated with ocular features (Q55789272) 1
Yes autoimmune disease (Q8084905) 1
Yes Peutz-Jeghers polyp (Q55950136) 1
Yes hypoxanthine-guanine phosphoribosyltransferase deficiency (Q56013793) 1
Yes familial chylomicronemia syndrome (Q56014181) 1
Yes hypergonadotropic hypogonadism (Q5958036) 1
Yes polycystic kidney disease (Q60195313) 1
Yes glomerulonephritis (Q605006) 1
Yes vein disorder (Q7918687) 1
Yes Ohtahara syndrome (Q649602) 1
Yes syndrome with a symptomatic strabismus (Q55789247) 1
Yes pervasive developmental disorder (Q6691991) 1
Yes urticarial syndrome (Q7901363) 1
Yes classical lissencephalies and subcortical band heterotopias (Q67215740) 1
Yes lysosomal storage disease (Q675010) 1
Yes Mannosidosis (Q6750947) 1
Yes Thyroid dyshormonogenesis (Q7799748) 1
Yes hyperlipoproteinemia type I (Q68640538) 1
Yes spinal muscular atrophies (Q7577466) 1
Yes spinal disease (Q7577457) 1
Yes mitochondrial encephalomyopathy (Q6881866) 1
Yes muscular disease (Q692536) 1
Yes overgrowth syndrome (Q7113674) 1
Yes pigmentation disorder (Q7193408) 1
Yes congenital disorder (Q727096) 1
Yes rare disease with odontological manifestation (Q55789054) 1
Yes other metabolic disease with skin involvement (Q55788569) 1
Yes dystonia (Q906492) 1
Yes inherited epidermolysis bullosa (Q55788582) 1
Yes mixed dermis disorder (Q55788599) 1
Yes other dermis disorder (Q55788600) 1
Yes skin tumor or hamartoma (Q55788604) 1
Yes mucopolysaccharidosis with skin involvement (Q55788606) 1
Yes syndromic lymphedema (Q55788697) 1
Yes spinocerebellar ataxia (Q899726) 1
Yes sialuria (Q7506696) 1
Yes blood coagulation disease (Q890200) 1
Yes primary osteolysis (Q55788819) 1
Yes familial cystic renal disease (Q55788849) 1
Yes hematological disorder with renal involvement (Q55788858) 1
Yes oligosaccharidosis (Q55788568) 1
Yes genetic lipodystrophy (Q55789109) 1
Yes constitutional hemolytic anemia due to acanthocytosis (Q55789124) 1
Yes genetic peripheral neuropathy (Q55789138) 1
Yes secondary ectropion (Q55789166) 1
Yes syndromic epicanthus (Q55789170) 1
Yes pigmented conjunctival lesion (Q55789203) 1
Yes syndromic myopia (Q55789206) 1
Yes cataract associated with a metabolic disease (Q55789224) 1
Yes cerebral disease with cataract (Q55789225) 1
Yes renal disease with cataract (Q55789226) 1
Yes musculoskeletal disease with cataract (Q55789228) 1
Yes lens shape anomaly (Q55789234) 1
Yes unclassified primitive or secondary maculopathy (Q55789241) 1
Yes retinal cancer (Q18556412) 1
Yes distal arthrogryposis (Q18553375) 1
Yes X-linked disease (Q18553438) 1
Yes syndromic intellectual disability (Q18553536) 1
Yes autoimmune disease of central nervous system (Q18553585) 1
Yes intrinsic cardiomyopathy (Q18553611) 1
Yes migraine with aura (Q18553762) 1
Yes eyelid degenerative disease (Q18553781) 1
Yes autonomic nervous system disease (Q18554088) 1
Yes sex differentiation disease (Q18554938) 1
Yes inherited blood coagulation disease (Q18555031) 1
Yes plasma protein metabolism disease (Q18555057) 1
Yes neuroaxonal dystrophy (Q18555065) 1
Yes iris disease (Q18555070) 1
Yes hepatic vascular disease (Q18555173) 1
Yes myotonic disease (Q18556352) 1
Yes thalassemia (Q185137) 1
Yes proliferative glomerulonephritis (Q18556474) 1
Yes aortic disease (Q18556675) 1
Yes muscle tissue disease (Q18557307) 1
Yes retinal cell cancer (Q18557709) 1
Yes myopathy of extraocular muscle (Q18558093) 1
Yes X-linked chondrodysplasia punctata (Q18987139) 1
Yes demyelinating disease of central nervous system (Q19000726) 1
Yes copper metabolism disease (Q19001238) 1
Yes sulfuraminoacidemia (Q19001322) 1
Yes chronic progressive external ophthalmoplegia (Q2026857) 1
Yes polyposis (Q2103081) 1
Yes synostosis (Q2141048) 1
Yes diabetes insipidus (Q220551) 1
Yes tremor (Q223907) 1
Yes pseudohermaphroditism (Q2273662) 1
Yes neutropenia (Q1435822) 1
Yes tubulopathy (Q1048573) 1
Yes cerebral calcification (Q108404609) 1
Yes Collagen VI myopathy (Q109676398) 1
Yes inherited tumor (Q1117773) 1
Yes tyrosinemia (Q1122668) 1
Yes congenital myopathy (Q112412) 1
Yes impaired renal function disease (Q11612288) 1
Yes myoclonus (Q116275) 1
Yes demyelinating disease (Q1186703) 1
Yes monogenic disease (Q1225194) 1
Yes distichia (Q1229478) 1
Yes vascular disease (Q1266890) 1
Yes congenital muscular dystrophy (Q1321884) 1
Yes severe combined immunodeficiency (Q1334408) 1
Yes myositis (Q1433212) 1
Yes primordial dwarfism (Q2289761) 1
Yes autism spectrum disorder (Q1436063) 1
Yes multiple endocrine neoplasia (Q1553018) 1
Yes hemophagocytic lymphohistiocytosis (Q1642170) 1
Yes hyperthyroidism (Q16499) 1
Yes dilated cardiac chambers (Q16644209) 1
Yes neurodegeneration with brain iron accumulation (Q16892735) 1
Yes cerebral creatine deficiency syndrome (Q16908143) 1
Yes generalized epilepsy with febrile seizures plus (Q16909671) 1
Yes neuro-cardio-facial-cutaneous syndromes (Q17074582) 1
Yes neuronal migration disorder (Q17146964) 1
Yes neurodegeneration (Q1755122) 1
Yes inherited metabolic disorder (Q1758393) 1
Yes connective tissue disease (Q1779300) 1
Yes strabismus (Q179951) 1
Yes atriodigital dysplasia (Q18018497) 1
Yes syndromic diaphragmatic or abdominal wall malformation (Q55785334) 1
Yes congenital hypothyroidism (Q531012) 1
Yes complete generalized lipodystrophy (Q53661801) 1
Yes eye abnormalities (Q54911717) 1
Yes TDP-43 Proteinopathies (Q54920211) 1
Yes malformations of cortical development, Group III (Q55003193) 1
Yes X-linked dominant disease (Q55010089) 1
Yes retinal disease (Q550455) 1
Yes Huntington disease and related disorders (Q55345637) 1
Yes PLA2G6-associated neurodegeneration (Q55346017) 1
Yes autosomal dominant cerebellar ataxia type IV (Q55346089) 1
Yes autosomal recessive degenerative and progressive cerebellar ataxia (Q55346094) 1
Yes frontotemporal degeneration with dementia (Q55346097) 1
Yes X-linked complex spastic paraplegia (Q55346104) 1
Yes multiple polyglandular tumor (Q55785235) 1
Yes constitutional neutropenia (Q55785274) 1
Yes SC phocomelia syndrome (Q52956039) 1
Yes syndrome with a central nervous system malformation as major feature (Q55785338) 1
Yes autosomal recessive hereditary sensory and autonomic neuropathy (Q55785425) 1
Yes rare syndrome with cardiac malformations (Q55785518) 1
Yes rare genetic respiratory disease (Q55785522) 1
Yes chromosomal anomaly with epilepsy as a major feature (Q55785627) 1
Yes cerebral malformation with epilepsy (Q55785630) 1
Yes DNA repair defect other than combined T-cell and B-cell immunodeficiencies (Q55785655) 1
Yes congenital myopathy with cores (Q55785700) 1
Yes syndromic hypothyroidism (Q55785710) 1
Yes syndrome with hypoparathyroidism (Q55785800) 1
Yes primary orthostatic hypotension (Q55785810) 1
Yes syndromic neurometabolic disease with non-X-linked intellectual disability (Q55785813) 1
Yes inherited skin tumor (Q55785837) 1
Yes genetic photodermatosis (Q55785838) 1
Yes genetic central nervous system and retinal vascular disease (Q55785839) 1
Yes metal metabolism disorder (Q3281373) 1
Yes sphingolipidosis (Q2309612) 1
Yes synucleinopathy (Q2376264) 1
Yes tauopathy (Q2397106) 1
Yes ocular cancer (Q2420648) 1
Yes Huntington's disease-like syndrome (Q24977062) 1
Yes tumor of hematopoietic and lymphoid tissues (Q2509220) 1
Yes dissection (Q2660911) 1
Yes porphyria (Q271759) 1
Yes hypomyelinating leukodystrophy (Q28065591) 1
Yes neonatal diabetes mellitus (Q2898645) 1
Yes channelopathy (Q2936142) 1
Yes photodermatosis (Q2986815) 1
Yes retinal degeneration (Q3043268) 1
Yes hemiplegic migraine (Q30587719) 1
Yes motor neuron disease (Q3221083) 1
Yes inherited renal tubular disease (Q55785848) 1
Yes inborn errors of purine–pyrimidine metabolism (Q3281375) 1
Yes ELANE-related neutropenia (Q3338731) 1
Yes lung disease (Q3392853) 1
Yes neurodevelopmental disorder (Q3450985) 1
Yes trinucleotide repeat disorder (Q356736) 1
Yes intrahepatic cholestasis (Q3682587) 1
Yes hereditary sensory and autonomic neuropathy (Q3702898) 1
Yes immune disorder (Q3843811) 1
Yes lymphoproliferative disorders (Q4165484) 1
Yes porphyria due to ALAD deficiency (Q419897) 1
Yes aging-associated disease (Q438962) 1
Yes hemangioblastoma (Q460937) 1
Yes basal ganglia disease (Q4866181) 1
Yes craniofacial disease (Q5182134) 1

"Single value" violations

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Violations count: 10

"Unique value" violations

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Violations count: 5

"Entity types" violations

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Violations count: 0

"Scope" violations

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Violations count: 0

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