AtlasTræk
Hypopituitarism
Resumé
AtlasDenne side som data
Tilføj .json til sidens adresse, eller bed om application/json, for at læse den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/hypopituitarism.json"
page <- fromJSON(url)
page$trait$nameLæs de gener, der er knyttet til Hypopituitarism, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test31 condition reports read genes linked to this trait
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.
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 10 of these genesFOXA2GLI2HESX1LHX4OTX2POU1F1About this report →
- Shwachman-Diamond SyndromeReads 2 of these genesEFL1SBDSAbout this report →
- Hypogonadotropic HypogonadismReads 8 of these genesFOXA2HESX1LHX4OTX2POU1F1PROP1About this report →
- Acromelic Frontonasal DysostosisReads 1 of these genesZSWIM6About this report →
Show 27 more reports
- CTNNB1 SyndromeReads 1 of these genesCTNNB1About this report →
- FrontorhinyReads 1 of these genesALX3About this report →
- Greig Cephalopolysyndactyly SyndromeReads 1 of these genesGLI3About this report →
- Sickle Cell DiseaseReads 1 of these genesHBBAbout this report →
- X-linked Autoinflammatory DiseaseReads 1 of these genesIKBKGAbout this report →
- Familial Isolated Pituitary Adenoma (FIPA / X-LAG)Reads 1 of these genesGPR101About this report →
- HypertriglyceridemiaReads 1 of these genesAPOA5About this report →
- 46,XX Differences of Sex DevelopmentReads 1 of these genesSOX3About this report →
- Ectodermal DysplasiasReads 2 of these genesIKBKGNFKBIAAbout this report →
- Hereditary Methaemoglobinaemia and Unstable HaemoglobinsReads 1 of these genesHBBAbout this report →
- ThalassaemiaReads 1 of these genesHBBAbout this report →
- Rare Inherited Bone Marrow Failure SyndromesReads 1 of these genesDNAJC21About this report →
- VitreoretinopathyReads 2 of these genesCTNNB1IKBKGAbout this report →
- Hereditary Sideroblastic AnaemiasReads 1 of these genesPUS1About this report →
- PolycythemiaReads 1 of these genesHBBAbout this report →
- Meckel SyndromeReads 1 of these genesTMEM67About this report →
- HyperinsulinismReads 1 of these genesFOXA2About this report →
- HyperlipidemiaReads 1 of these genesAPOA5About this report →
- Nephronophthisis and Senior-Løken SyndromeReads 1 of these genesTMEM67About this report →
- Noonan SyndromeReads 1 of these genesBRAFAbout this report →
- Other Inborn Errors of ImmunityReads 3 of these genesIKBKGNFKBIASBDSAbout this report →
- Microphthalmia, Anophthalmia & ColobomaReads 1 of these genesOTX2About this report →
- Joubert Syndrome And Related DisordersReads 1 of these genesTMEM67About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesTMEM67About this report →
- Intellectual DisabilityReads 2 of these genesSOX3CTNNB1About this report →
- Hypertrophic CardiomyopathyReads 1 of these genesBRAFAbout this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesTMEM67About this report →
Læs de gener, der er knyttet til Hypopituitarism, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test28 gener knyttet til Hypopituitarism
Ændringer i disse gener forårsager sjældne tilstande, hvor Hypopituitarism 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 |
|---|---|---|
| FAAP100FA core complex associated protein 100 | Altid | I 1 tilstand |
| FARSAphenylalanyl-tRNA synthetase subunit alpha | Altid | I 1 tilstand |
| FOXA2forkhead box A2 | Altid | I 1 tilstand |
| GLI2GLI family zinc finger 2 | Altid | I 2 tilstande |
| GPR101G protein-coupled receptor 101 | Altid | I 1 tilstand |
| HESX1HESX homeobox 1 | Altid | I 2 tilstande |
| LHX4LIM homeobox 4 | Altid | I 2 tilstande |
| OTX2orthodenticle homeobox 2 | Altid | I 1 tilstand |
| POU1F1POU class 1 homeobox 1 | Altid | I 3 tilstande |
| PROP1PROP paired-like homeobox 1 | Altid | I 3 tilstande |
| PTBP1polypyrimidine tract binding protein 1 | Altid | I 1 tilstand |
| SOX3SRY-box transcription factor 3 | Altid | I 1 tilstand |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Meget ofte (80–99 %) | I 1 tilstand |
| CTNNB1catenin beta 1 | Meget ofte (80–99 %) | I 1 tilstand |
| TMEM67transmembrane protein 67 | Meget ofte (80–99 %) | I 1 tilstand |
| GLI3GLI family zinc finger 3 | Ofte (30–79 %) | I 1 tilstand |
| LHX3LIM homeobox 3 | Ofte (30–79 %) | I 1 tilstand |
| MANFmesencephalic astrocyte derived neurotrophic factor | Ofte (30–79 %) | I 1 tilstand |
| PUS1pseudouridine synthase 1 | Ofte (30–79 %) | I 1 tilstand |
| ZSWIM6zinc finger SWIM-type containing 6 | Ofte (30–79 %) | I 2 tilstande |
| ALX3ALX homeobox 3 | Nogle gange (5–29 %) | I 1 tilstand |
| HBBhemoglobin subunit beta | Nogle gange (5–29 %) | I 2 tilstande |
| IKBKGinhibitor of nuclear factor kappa B kinase regulatory subunit gamma | Nogle gange (5–29 %) | I 1 tilstand |
| NFKBIANFKB inhibitor alpha | Nogle gange (5–29 %) | I 1 tilstand |
| DNAJC21DnaJ heat shock protein family (Hsp40) member C21 | Sjældent (1–4%) | I 1 tilstand |
| EFL1elongation factor like GTPase 1 | Sjældent (1–4%) | I 1 tilstand |
| SBDSSBDS ribosome maturation factor | Sjældent (1–4%) | I 1 tilstand |
| APOA5apolipoprotein A5 | 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.
Snævrere træk
Bredere træk
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 2026.10.19-9814e911.
AtlasFrom traits to your genome
Read the genes behind these traits in your own DNA.
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