AtlasEgenskap
Small thyroid gland
Klinisk navn: Thyroid hypoplasia
Developmental hypoplasia of the thyroid gland.
Sammendrag
- Også kalt
- Hypoplastic thyroid
- 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/thyroid-hypoplasia.json"
page <- fromJSON(url)
page$trait$nameLes genene knyttet til Small thyroid gland, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test20 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.
- Treacher Collins SyndromeReads 4 of these genesPOLR1BPOLR1CPOLR1DTCOF1About this report →
- Congenital HypothyroidismReads 8 of these genesPAX8SLC26A4TSHBTSHRIRS4TRHRAbout this report →
- Thyroid CancerReads 8 of these genesPAX8SLC26A4TSHBTSHRIRS4TRHRAbout this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 6 of these genesHESX1LHX3LHX4POU1F1PROP1GLI3About this report →
Show 16 more reports
- Greig Cephalopolysyndactyly SyndromeReads 1 of these genesGLI3About this report →
- KAT6B-Related DisordersReads 1 of these genesKAT6BAbout this report →
- Pendred SyndromeReads 1 of these genesSLC26A4About this report →
- POLR1C-Related DisorderReads 1 of these genesPOLR1CAbout this report →
- Kabuki SyndromeReads 1 of these genesKMT2DAbout this report →
- Hypogonadotropic HypogonadismReads 5 of these genesHESX1LHX3LHX4POU1F1PROP1About this report →
- HyperthyroidismReads 1 of these genesTSHRAbout this report →
- Tetralogy of FallotReads 1 of these genesNKX2-5About this report →
- Syndromic and Metabolic CardiomyopathiesReads 1 of these genesNKX2-5About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesNKX2-5About this report →
- Inherited IchthyosesReads 1 of these genesNSDHLAbout this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 1 of these genesPOLR1CAbout this report →
- Other Inherited LeukodystrophiesReads 1 of these genesPOLR1CAbout this report →
- Hearing Loss and DeafnessReads 1 of these genesSLC26A4About this report →
- Intellectual DisabilityReads 1 of these genesNSDHLAbout this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesPOLR1CAbout this report →
Les genene knyttet til Small thyroid gland, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test23 gener knyttet til Small thyroid gland
Endringer i disse genene forårsaker sjeldne tilstander der Small thyroid gland 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 |
|---|---|---|
| PAX8paired box 8 | Svært ofte (80–99 %) | I 2 tilstander |
| SLC26A4solute carrier family 26 member 4 | Svært ofte (80–99 %) | I 1 tilstand |
| TSHBthyroid stimulating hormone subunit beta | Svært ofte (80–99 %) | I 1 tilstand |
| TSHRthyroid stimulating hormone receptor | Svært ofte (80–99 %) | I 2 tilstander |
| ADAMTSL1ADAMTS like 1 | Ofte (30–79 %) | I 1 tilstand |
| HESX1HESX homeobox 1 | Ofte (30–79 %) | I 1 tilstand |
| IRS4insulin receptor substrate 4 | Ofte (30–79 %) | I 1 tilstand |
| KAT6Blysine acetyltransferase 6B | Ofte (30–79 %) | I 1 tilstand |
| LHX3LIM homeobox 3 | Ofte (30–79 %) | I 1 tilstand |
| LHX4LIM homeobox 4 | Ofte (30–79 %) | I 1 tilstand |
| POU1F1POU class 1 homeobox 1 | Ofte (30–79 %) | I 1 tilstand |
| PROP1PROP paired-like homeobox 1 | Ofte (30–79 %) | I 1 tilstand |
| TRHRthyrotropin releasing hormone receptor | Ofte (30–79 %) | I 1 tilstand |
| GLI3GLI family zinc finger 3 | Noen ganger (5–29 %) | I 1 tilstand |
| GNB2G protein subunit beta 2 | Noen ganger (5–29 %) | I 1 tilstand |
| KMT2Dlysine methyltransferase 2D | Noen ganger (5–29 %) | I 1 tilstand |
| NSDHLNAD(P) dependent 3-beta-hydroxysteroid dehydrogenase NSDHL | Noen ganger (5–29 %) | I 1 tilstand |
| POLR1BRNA polymerase I subunit B | Noen ganger (5–29 %) | I 1 tilstand |
| POLR1CRNA polymerase I and III subunit C | Noen ganger (5–29 %) | I 1 tilstand |
| POLR1DRNA polymerase I and III subunit D | Noen ganger (5–29 %) | I 1 tilstand |
| TCOF1treacle ribosome biogenesis factor 1 | Noen ganger (5–29 %) | I 1 tilstand |
| DUOX2dual oxidase 2 | Sjelden (1–4%) | I 1 tilstand |
| NKX2-5NK2 homeobox 5 | 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.
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 2026.10.18-8b139e39.
AtlasFrom traits to your genome
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