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Abnormal fear-induced behavior
An abnormal fear-induced behavior includes observable actions. This behavior is characterized by abnormal responses to fear or abnormal fear levels. Examples of such behavior include avoiding fear-inducing situations.
Resumé
- Også kaldet
- Abnormal fear/anxiety-related behavior, Abnormal fear/anxiety-related behaviour
- Kropssystem
- Abnormality of the nervous system
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library(jsonlite)
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page$trait$nameLæs de gener, der er knyttet til Abnormal fear-induced behavior, og resten af dit genom, med én test.
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Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Rett Syndrome and MECP2-Related DisordersReads 1 of these genesMECP2About this report →
- Familial Isolated Pituitary Adenoma (FIPA / X-LAG)Reads 1 of these genesAIPAbout this report →
- Sandhoff Disease and GM2 Activator DeficiencyReads 1 of these genesGM2AAbout this report →
- Hepatic Porphyria DisordersReads 1 of these genesALADAbout this report →
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- PorphyriaReads 1 of these genesALADAbout this report →
- Intellectual DisabilityReads 3 of these genesCREBBPEP300MECP2About this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 1 of these genesFIG4About this report →
- Lysosomal Storage DiseaseReads 1 of these genesGM2AAbout this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesFIG4About this report →
- Inherited Neurodegenerative DisordersReads 2 of these genesGM2AFIG4About this report →
- Epilepsy (Full Panel)Reads 1 of these genesMECP2About this report →
- Rare Hereditary Peripheral NeuropathiesReads 1 of these genesFIG4About this report →
Læs de gener, der er knyttet til Abnormal fear-induced behavior, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test8 gener knyttet til Abnormal fear-induced behavior
Ændringer i disse gener forårsager sjældne tilstande, hvor Abnormal fear-induced behavior ses. De fleste med dette træk har ingen af disse tilstande, og et gen på denne liste siger intet om nogens eget genom.
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| GM2Aganglioside GM2 activator | Meget ofte (80–99 %) | I 1 tilstand |
| CREBBPCREB binding lysine acetyltransferase | Ofte (30–79 %) | I 2 tilstande |
| EP300EP300 lysine acetyltransferase | Ofte (30–79 %) | I 1 tilstand |
| ALADaminolevulinate dehydratase | Nogle gange (5–29 %) | I 1 tilstand |
| FIG4FIG4 phosphoinositide 5-phosphatase | Nogle gange (5–29 %) | I 1 tilstand |
| MECP2methyl-CpG binding protein 2 | Nogle gange (5–29 %) | I 1 tilstand |
| AIPAHR interacting HSP90 co-chaperone | Ikke registreret | I 1 tilstand |
| USP8ubiquitin specific peptidase 8 | Ikke registreret | I 1 tilstand |
Hvor hyppigt det ses hos personer med en af genets tilstande, den hyppigste værdi på tværs af dem, sådan som Human Phenotype Ontology registrerer det. Disse sider beskriver egenskaber og den forskning, der ligger bag dem. De er ikke en diagnose, og hvis du har spørgsmål om symptomer, bør du spørge en læge eller genetisk rådgiver.
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Hvor oplysningerne kommer fra
- Human Phenotype Ontology, udgivelse 2026-09-01: egenskaben, dens navne, definition og de gener, der er knyttet til den. Læs mere på hpo.jax.org.
- Dataudgivelse 2026.10.21-777c9289.
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