AtlasEgenskap
Hypopituitarism
Sammendrag
AtlasDenne siden som data
Legg til .json etter adressen til siden, eller be om application/json, for å lese den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/hypopituitarism.json"
page <- fromJSON(url)
page$trait$nameLes genene knyttet til Hypopituitarism, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt 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 →
Les genene knyttet til Hypopituitarism, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test28 gener knyttet til Hypopituitarism
Endringer i disse genene forårsaker sjeldne tilstander der Hypopituitarism forekommer. De fleste med denne egenskapen har ingen av disse tilstandene, og et gen på denne listen sier ingenting om noens eget genom.
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| FAAP100FA core complex associated protein 100 | Alltid | I 1 tilstand |
| FARSAphenylalanyl-tRNA synthetase subunit alpha | Alltid | I 1 tilstand |
| FOXA2forkhead box A2 | Alltid | I 1 tilstand |
| GLI2GLI family zinc finger 2 | Alltid | I 2 tilstander |
| GPR101G protein-coupled receptor 101 | Alltid | I 1 tilstand |
| HESX1HESX homeobox 1 | Alltid | I 2 tilstander |
| LHX4LIM homeobox 4 | Alltid | I 2 tilstander |
| OTX2orthodenticle homeobox 2 | Alltid | I 1 tilstand |
| POU1F1POU class 1 homeobox 1 | Alltid | I 3 tilstander |
| PROP1PROP paired-like homeobox 1 | Alltid | I 3 tilstander |
| PTBP1polypyrimidine tract binding protein 1 | Alltid | I 1 tilstand |
| SOX3SRY-box transcription factor 3 | Alltid | I 1 tilstand |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Svært ofte (80–99 %) | I 1 tilstand |
| CTNNB1catenin beta 1 | Svært ofte (80–99 %) | I 1 tilstand |
| TMEM67transmembrane protein 67 | Svært 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 tilstander |
| ALX3ALX homeobox 3 | Noen ganger (5–29 %) | I 1 tilstand |
| HBBhemoglobin subunit beta | Noen ganger (5–29 %) | I 2 tilstander |
| IKBKGinhibitor of nuclear factor kappa B kinase regulatory subunit gamma | Noen ganger (5–29 %) | I 1 tilstand |
| NFKBIANFKB inhibitor alpha | Noen ganger (5–29 %) | I 1 tilstand |
| DNAJC21DnaJ heat shock protein family (Hsp40) member C21 | Sjelden (1–4%) | I 1 tilstand |
| EFL1elongation factor like GTPase 1 | Sjelden (1–4%) | I 1 tilstand |
| SBDSSBDS ribosome maturation factor | Sjelden (1–4%) | I 1 tilstand |
| APOA5apolipoprotein A5 | Ikke registrert | I 1 tilstand |
Hvor ofte dette forekommer hos personer med en av genets tilstander, oppgitt som den hyppigste forekomsten blant dem, slik Human Phenotype Ontology registrerer den. Disse sidene beskriver egenskaper og forskningen bak dem. De er ikke en diagnose, og om symptomer bør du spørre lege eller genetisk rådgiver.
Smalere egenskaper
Bredere egenskaper
Slik er informasjonen samlet
- Human Phenotype Ontology, versjon 2026-09-01: egenskapen, navnene på den, definisjonen og genene som er knyttet til den. Les mer på hpo.jax.org.
- Datautgave 2026.10.19-9814e911.
AtlasFrom traits to your genome
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