AtlasEgenskap
Central hypothyroidism
A type of hypothyroidism due to an insufficient stimulation of an otherwise normal thyroid gland. Central hypothyroidism is caused by either pituitary (secondary hypothyroidism) or hypothalamic (tertiary hypothyroidism) defects.
Sammendrag
- Kroppssystem
- Abnormality of the endocrine system
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/central-hypothyroidism.json"
page <- fromJSON(url)
page$trait$nameLes genene knyttet til Central hypothyroidism, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test19 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 11 of these genesGLI2OTX2ROBO1CDONDISP1PLCH1About this report →
- DLL1-Related Neurodevelopmental DisorderReads 1 of these genesDLL1About this report →
- Hypogonadotropic HypogonadismReads 7 of these genesOTX2ROBO1CPEMAGEL2SNRPNFGF8About this report →
- Nevoid Basal Cell Carcinoma (Gorlin) SyndromeReads 1 of these genesPTCH1About this report →
Show 15 more reports
- Severe Inherited Insulin ResistanceReads 1 of these genesINSRAbout this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 2 of these genesMAGEL2SNRPNAbout this report →
- Congenital HypothyroidismReads 2 of these genesIRS4TBL1XAbout this report →
- Cornelia de Lange SyndromeReads 1 of these genesSMC1AAbout this report →
- Microphthalmia, Anophthalmia & ColobomaReads 2 of these genesOTX2SHHAbout this report →
- Monogenic Obesity (Leptin-Melanocortin Pathway)Reads 1 of these genesSIM1About this report →
- Thyroid CancerReads 2 of these genesIRS4TBL1XAbout this report →
- Oculocutaneous AlbinismReads 1 of these genesOCA2About this report →
- Heterotaxy & Laterality DefectsReads 1 of these genesNODALAbout this report →
- HyperinsulinismReads 1 of these genesINSRAbout this report →
- Autosomal Recessive Primary MicrocephalyReads 1 of these genesSTILAbout this report →
- Epilepsy (Full Panel)Reads 3 of these genesDMXL2NEXMIFSMC1AAbout this report →
- Syndromic CraniosynostosisReads 1 of these genesFGFR1About this report →
- Intellectual DisabilityReads 3 of these genesNEXMIFRPL10SETBP1About this report →
- Joubert Syndrome And Related DisordersReads 1 of these genesKATNIPAbout this report →
Les genene knyttet til Central hypothyroidism, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test39 gener knyttet til Central hypothyroidism
Endringer i disse genene forårsaker sjeldne tilstander der Central hypothyroidism 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 |
|---|---|---|
| DMXL2Dmx like 2 | Alltid | I 2 tilstander |
| GLI2GLI family zinc finger 2 | Alltid | I 5 tilstander |
| NINninein | Alltid | I 1 tilstand |
| OTX2orthodenticle homeobox 2 | Alltid | I 1 tilstand |
| ROBO1roundabout guidance receptor 1 | Alltid | I 1 tilstand |
| SEL1LSEL1L adaptor subunit of SYVN1 ubiquitin ligase | Alltid | I 1 tilstand |
| CPEcarboxypeptidase E | Ofte (30–79 %) | I 1 tilstand |
| MAGEL2MAGE family member L2 | Ofte (30–79 %) | I 4 tilstander |
| NDNnecdin, MAGE family member | Ofte (30–79 %) | I 3 tilstander |
| NEXMIFneurite extension and migration factor | Ofte (30–79 %) | I 1 tilstand |
| OCA2OCA2 melanosomal transmembrane protein | Ofte (30–79 %) | I 3 tilstander |
| RPL10ribosomal protein L10 | Ofte (30–79 %) | I 1 tilstand |
| SNRPNsmall nuclear ribonucleoprotein polypeptide N | Ofte (30–79 %) | I 3 tilstander |
| CDONcell adhesion associated, oncogene regulated | Noen ganger (5–29 %) | I 4 tilstander |
| CRIPTOcripto, EGF-CFC family member | Noen ganger (5–29 %) | I 4 tilstander |
| DISP1dispatched RND transporter family member 1 | Noen ganger (5–29 %) | I 4 tilstander |
| DLL1delta like canonical Notch ligand 1 | Noen ganger (5–29 %) | I 4 tilstander |
| EIF2AK3eukaryotic translation initiation factor 2 alpha kinase 3 | Noen ganger (5–29 %) | I 1 tilstand |
| FGF8fibroblast growth factor 8 | Noen ganger (5–29 %) | I 4 tilstander |
| FGFR1fibroblast growth factor receptor 1 | Noen ganger (5–29 %) | I 2 tilstander |
| FOXH1forkhead box H1 | Noen ganger (5–29 %) | I 4 tilstander |
| GAS1growth arrest specific 1 | Noen ganger (5–29 %) | I 4 tilstander |
| GNAQG protein subunit alpha q | Noen ganger (5–29 %) | I 1 tilstand |
| INSRinsulin receptor | Noen ganger (5–29 %) | I 1 tilstand |
| NODALnodal growth differentiation factor | Noen ganger (5–29 %) | I 4 tilstander |
| PLCH1phospholipase C eta 1 | Noen ganger (5–29 %) | I 1 tilstand |
| PTCH1patched 1 | Noen ganger (5–29 %) | I 4 tilstander |
| SHHsonic hedgehog signaling molecule | Noen ganger (5–29 %) | I 4 tilstander |
| SIM1SIM bHLH transcription factor 1 | Noen ganger (5–29 %) | I 1 tilstand |
| SIX3SIX homeobox 3 | Noen ganger (5–29 %) | I 4 tilstander |
| SMC1Astructural maintenance of chromosomes 1A | Noen ganger (5–29 %) | I 1 tilstand |
| STAG2STAG2 cohesin complex component | Noen ganger (5–29 %) | I 2 tilstander |
| STILSTIL centriolar assembly protein | Noen ganger (5–29 %) | I 4 tilstander |
| TGIF1TGFB induced factor homeobox 1 | Noen ganger (5–29 %) | I 4 tilstander |
| ZIC2Zic family zinc finger 2 | Noen ganger (5–29 %) | I 4 tilstander |
| SETBP1SET binding protein 1 | Sjelden (1–4%) | I 1 tilstand |
| IRS4insulin receptor substrate 4 | Ikke registrert | I 1 tilstand |
| KATNIPkatanin interacting protein | Ikke registrert | I 1 tilstand |
| TBL1Xtransducin beta like 1 X-linked | 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.
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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.
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