AtlasKeitä autammeTieteemmeTuotteetTulokset
Kirjaudu sisäänKysySekvensoi genomisi↗
Piirre
Development of small head that was not present at birth
Kliininen nimi: Secondary microcephaly
Head circumference which falls below 2 standard deviations below the mean for age and gender because of insufficient head growth after birth.
Yhteenveto
- Tunnetaan myös nimellä
- Acquired microcephaly, Deceleration of head growth, Microcephaly, acquired, Microcephaly, postnatal, Postnatal deceleration of head circumference, Postnatal microcephaly
AtlasKeitä autammeTieteemmeTuotteetTulokset
Kirjaudu sisäänKysySekvensoi genomisi↗
Tämä sivu datana
Lisää sivun osoitteen perään .json tai pyydä application/json-muotoa, niin saat sivun JSON-muodossa.
library(jsonlite)
url <- "https://dantelabs.com/traits/secondary-microcephaly.json"
page <- fromJSON(url)
page$trait$nameKeitä autammeTieteemmeTuotteetTulokset
Kirjaudu sisäänKysySekvensoi genomisi↗
Lue Development of small head that was not present at birth-nimiseen tai sen kanssa liittyvät geenit ja muu genomisi yhdellä testillä.
Alkaen 449 $Ilmainen toimitus · Tulokset 6–8 viikossa
Tilaa Genome Test63 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.
- Epilepsy (Full Panel)Reads 32 of these genesADAM22BRAT1DNM1EEF1A2FGF12GABRA5About this report →
- Lissencephaly Spectrum DisordersReads 8 of these genesRAB18TBC1D20ACTG1CTNNA2DCXPAFAH1B1About this report →
- Encephalopathy due to Mitochondrial and Peroxisomal Fission DefectReads 2 of these genesDNM1LMFFAbout this report →
- Intellectual DisabilityReads 19 of these genesTCF4TRAPPC9EP300CERT1CREBBPDYRK1AAbout this report →
Show 59 more reports
- Familial Hemiplegic MigraineReads 2 of these genesATP1A2SCN1AAbout this report →
- Disorders of Glycine & Serine MetabolismReads 3 of these genesGCSHSLC1A4PSAT1About this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 5 of these genesHSPD1PYCR2HIKESHIDEGS1VPS11About this report →
- 3-Methylglutaconic Aciduria Type 8 (HTRA2)Reads 1 of these genesHTRA2About this report →
- Angelman SyndromeReads 1 of these genesUBE3AAbout this report →
- ATP1A2-Related Fetal Akinesia with PolymicrogyriaReads 1 of these genesATP1A2About this report →
- BCKDK DeficiencyReads 1 of these genesBCKDKAbout this report →
- BRAT1-Related Neurodevelopmental Disorder with Cerebellar AtrophyReads 1 of these genesBRAT1About this report →
- Christianson SyndromeReads 1 of these genesSLC9A6About this report →
- Dravet SyndromeReads 1 of these genesSCN1AAbout this report →
- FDXR-Related Mitochondrial DisorderReads 1 of these genesFDXRAbout this report →
- Glutaminase DeficiencyReads 1 of these genesGLSAbout this report →
- Jaberi-Elahi SyndromeReads 1 of these genesGTPBP2About this report →
- Mandibulofacial Dysostosis with MicrocephalyReads 1 of these genesEFTUD2About this report →
- Mowat-Wilson SyndromeReads 1 of these genesZEB2About this report →
- Neurooculocardiogenitourinary Syndrome (WDR37)Reads 1 of these genesWDR37About this report →
- NGLY1 DeficiencyReads 1 of these genesNGLY1About this report →
- Rett Syndrome and MECP2-Related DisordersReads 1 of these genesMECP2About this report →
- TRAPPC9-Related Intellectual DisabilityReads 1 of these genesTRAPPC9About this report →
- UBTF-Related NeuroregressionReads 1 of these genesUBTFAbout this report →
- UNC13A-Related Neurodevelopmental DisordersReads 1 of these genesUNC13AAbout this report →
- VPS11-Related LeukodystrophyReads 1 of these genesVPS11About this report →
- Cornelia de Lange SyndromeReads 2 of these genesSMC1ASMC3About this report →
- Congenital Disorders of GlycosylationReads 8 of these genesCOG2COG8PIGATMEM165DPM1COG6About this report →
- DOORS SyndromeReads 1 of these genesTBC1D24About this report →
- Hereditary Manganese Transporter DisordersReads 1 of these genesSLC39A14About this report →
- Rare Inherited Megaloblastic AnaemiasReads 1 of these genesDHFRAbout this report →
- Primary Mitochondrial DiseaseReads 8 of these genesATP5POFOXRED1C2orf69NDUFA11CRLS1PRORPAbout this report →
- Complex Neurodevelopmental Disorder With Motor FeaturesReads 2 of these genesCACNA1BEMC1About this report →
- Pontocerebellar Hypoplasia (TSEN54 and MINPP1)Reads 3 of these genesAMPD2VPS53CHMP1AAbout this report →
- Inherited Neurodegenerative DisordersReads 12 of these genesDNM1LGPT2HSPD1ITPR1PYCR2TBCDAbout this report →
- Microphthalmia, Anophthalmia & ColobomaReads 3 of these genesRAB18TBC1D20RAB3GAP2About this report →
- Other Inherited LeukodystrophiesReads 5 of these genesHSPD1PYCR2HIKESHIDEGS1VPS11About this report →
- Complex Cortical Dysplasia and Frontoparietal PolymicrogyriaReads 2 of these genesKIF5CCTNNA2About this report →
- MelanomaReads 1 of these genesCDK4About this report →
- Oculocutaneous AlbinismReads 1 of these genesOCA2About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 2 of these genesSLC18A2SLC2A1About this report →
- Anterior Segment Dysgenesis, Axenfeld-Rieger Syndrome & AniridiaReads 1 of these genesITPR1About this report →
- Rare Hereditary Peripheral NeuropathiesReads 5 of these genesFDXRFOXRED1MFFWARS1COQ9About this report →
- Hereditary Pheochromocytoma and ParagangliomaReads 1 of these genesSDHDAbout this report →
- BH4 Deficiency & Monoamine Neurotransmitter DisordersReads 1 of these genesSLC18A2About this report →
- Severe Congenital NeutropeniaReads 1 of these genesCLPBAbout this report →
- Hereditary Optic NeuropathyReads 1 of these genesDNM1LAbout this report →
- Neuronal Ceroid LipofuscinosisReads 1 of these genesPPT1About this report →
- Hereditary Spastic ParaplegiaReads 2 of these genesGPT2HSPD1About this report →
- Leigh SyndromeReads 2 of these genesFOXRED1MFFAbout this report →
- Hereditary Corneal DystrophiesReads 1 of these genesTCF4About this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPIGAAbout this report →
- Syndromic Complex Neurodevelopmental DisorderReads 1 of these genesRNU4-2About this report →
- Hearing Loss and DeafnessReads 2 of these genesACTG1TBC1D24About this report →
- Spinal Muscular AtrophyReads 1 of these genesWARS1About this report →
- Congenital Muscular DystrophiesReads 1 of these genesDPM2About this report →
- Inherited ThrombocytopeniasReads 1 of these genesRAP1BAbout this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 1 of these genesITPR1About this report →
- Dilated CardiomyopathyReads 1 of these genesDOLKAbout this report →
- Hypogonadotropic HypogonadismReads 1 of these genesRAB3GAP2About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesWWOXAbout this report →
- Lysosomal Storage DiseaseReads 1 of these genesPPT1About this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesWARS1About this report →
Lue Development of small head that was not present at birth-nimiseen tai sen kanssa liittyvät geenit ja muu genomisi yhdellä testillä.
Alkaen 449 $Ilmainen toimitus · Tulokset 6–8 viikossa
Tilaa Genome Test155 geeniä, jotka liittyvät piirteeseen Development of small head that was not present at birth
Näiden geenien muutokset aiheuttavat harvinaisia sairauksia, joissa Development of small head that was not present at birth esiintyy. Useimmilla, joilla on tämä piirre, ei ole mitään näistä sairauksista, eikä tämän listan geeni kerro mitään kenenkään omasta genomista.
| Geeni | Kuinka usein sitä esiintyy | Sairaudet |
|---|---|---|
| ADAM22ADAM metallopeptidase domain 22 | Aina | 1 sairaudessa |
| AMPD2adenosine monophosphate deaminase 2 | Aina | 1 sairaudessa |
| ARNT2aryl hydrocarbon receptor nuclear translocator 2 | Aina | 1 sairaudessa |
| ASPNATaspartate N-acetyltransferase | Aina | 1 sairaudessa |
| ATP5POATP synthase peripheral stalk subunit OSCP | Aina | 1 sairaudessa |
| BORCS8BLOC-1 related complex subunit 8 | Aina | 1 sairaudessa |
| BRAT1BRCA1 associated ATM activator 1 | Aina | 1 sairaudessa |
| CACNA1Bcalcium voltage-gated channel subunit alpha1 B | Aina | 1 sairaudessa |
| CDK4cyclin dependent kinase 4 | Aina | 1 sairaudessa |
| COG2component of oligomeric golgi complex 2 | Aina | 2 sairaudessa |
| COG8component of oligomeric golgi complex 8 | Aina | 1 sairaudessa |
| DNM1dynamin 1 | Aina | 1 sairaudessa |
| DNM1Ldynamin 1L | Aina | 1 sairaudessa |
| EEF1A2eukaryotic translation elongation factor 1 alpha 2 | Aina | 1 sairaudessa |
| EEFSECeukaryotic elongation factor, selenocysteine-tRNA specific | Aina | 1 sairaudessa |
| FDXRferredoxin reductase | Aina | 1 sairaudessa |
| FGF12fibroblast growth factor 12 | Aina | 1 sairaudessa |
| FOXRED1FAD dependent oxidoreductase domain containing 1 | Aina | 1 sairaudessa |
| FTOFTO alpha-ketoglutarate dependent dioxygenase | Aina | 1 sairaudessa |
| GABRA5gamma-aminobutyric acid type A receptor subunit alpha5 | Aina | 1 sairaudessa |
| GCSHglycine cleavage system protein H | Aina | 1 sairaudessa |
| GINS3GINS complex subunit 3 | Aina | 1 sairaudessa |
| GLSglutaminase | Aina | 1 sairaudessa |
| GON4Lgon-4 like | Aina | 1 sairaudessa |
| GPT2glutamic--pyruvic transaminase 2 | Aina | 1 sairaudessa |
| GTF3C3general transcription factor IIIC subunit 3 | Aina | 1 sairaudessa |
| GTPBP2GTP binding protein 2 | Aina | 1 sairaudessa |
| HSPD1heat shock protein family D (Hsp60) member 1 | Aina | 1 sairaudessa |
| IARS1isoleucyl-tRNA synthetase 1 | Aina | 1 sairaudessa |
| ITPR1inositol 1,4,5-trisphosphate receptor type 1 | Aina | 1 sairaudessa |
| JAM3junctional adhesion molecule 3 | Aina | 1 sairaudessa |
| JKAMPJNK1/MAPK8 associated membrane protein | Aina | 1 sairaudessa |
| KIF5Ckinesin family member 5C | Aina | 1 sairaudessa |
| MED17mediator complex subunit 17 | Aina | 1 sairaudessa |
| MFFmitochondrial fission factor | Aina | 2 sairaudessa |
| MOCS3molybdenum cofactor synthesis 3 | Aina | 1 sairaudessa |
| PARS2prolyl-tRNA synthetase 2, mitochondrial | Aina | 1 sairaudessa |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Aina | 1 sairaudessa |
| PTRH2peptidyl-tRNA hydrolase 2 | Aina | 2 sairaudessa |
| PYCR2pyrroline-5-carboxylate reductase 2 | Aina | 1 sairaudessa |
Näytä 115 geeniä lisää
| Geeni | Kuinka usein sitä esiintyy | Sairaudet |
|---|---|---|
| RAB18RAB18, member RAS oncogene family | Aina | 1 sairaudessa |
| RAP1BRAP1B, member of RAS oncogene family | Aina | 1 sairaudessa |
| RBSNrabenosyn, RAB effector | Aina | 1 sairaudessa |
| RFC4replication factor C subunit 4 | Aina | 1 sairaudessa |
| RNU2-2RNA, U2 small nuclear 2 | Aina | 1 sairaudessa |
| RNU6ATACRNA, U6atac small nuclear | Aina | 1 sairaudessa |
| SDHDsuccinate dehydrogenase complex subunit D | Aina | 1 sairaudessa |
| SLC25A22solute carrier family 25 member 22 | Aina | 1 sairaudessa |
| SUPT7LSPT7 like, STAGA complex subunit gamma | Aina | 1 sairaudessa |
| TAF2TATA-box binding protein associated factor 2 | Aina | 2 sairaudessa |
| TBC1D20TBC1 domain family member 20 | Aina | 1 sairaudessa |
| TBCDtubulin folding cofactor D | Aina | 2 sairaudessa |
| TCF4transcription factor 4 | Aina | 1 sairaudessa |
| TM2D3TM2 domain containing 3 | Aina | 1 sairaudessa |
| TMEM165transmembrane protein 165 | Aina | 1 sairaudessa |
| TOMM7translocase of outer mitochondrial membrane 7 | Aina | 1 sairaudessa |
| TRAPPC2Ltrafficking protein particle complex subunit 2L | Aina | 1 sairaudessa |
| TRAPPC9trafficking protein particle complex subunit 9 | Aina | 1 sairaudessa |
| UBE3Aubiquitin protein ligase E3A | Aina | 4 sairaudessa |
| VPS53VPS53 subunit of GARP complex | Aina | 1 sairaudessa |
| WARS1tryptophanyl-tRNA synthetase 1 | Aina | 1 sairaudessa |
| BCKDKbranched chain keto acid dehydrogenase kinase | Hyvin usein (80–99%) | 1 sairaudessa |
| C2orf69chromosome 2 open reading frame 69 | Hyvin usein (80–99%) | 1 sairaudessa |
| DPM1dolichyl-phosphate mannosyltransferase subunit 1, catalytic | Hyvin usein (80–99%) | 2 sairaudessa |
| EFTUD2elongation factor Tu GTP binding domain containing 2 | Hyvin usein (80–99%) | 1 sairaudessa |
| EP300EP300 lysine acetyltransferase | Hyvin usein (80–99%) | 1 sairaudessa |
| FRA10AC1FRA10A associated CGG repeat 1 | Hyvin usein (80–99%) | 1 sairaudessa |
| HIKESHIheat shock protein nuclear import factor hikeshi | Hyvin usein (80–99%) | 1 sairaudessa |
| MDGA2MAM domain containing glycosylphosphatidylinositol anchor 2 | Hyvin usein (80–99%) | 1 sairaudessa |
| OCA2OCA2 melanosomal transmembrane protein | Hyvin usein (80–99%) | 1 sairaudessa |
| PLPBPpyridoxal phosphate binding protein | Hyvin usein (80–99%) | 1 sairaudessa |
| SLC18A2solute carrier family 18 member A2 | Hyvin usein (80–99%) | 1 sairaudessa |
| UBA5ubiquitin like modifier activating enzyme 5 | Hyvin usein (80–99%) | 1 sairaudessa |
| UFC1ubiquitin-fold modifier conjugating enzyme 1 | Hyvin usein (80–99%) | 1 sairaudessa |
| UGGT1UDP-glucose glycoprotein glucosyltransferase 1 | Hyvin usein (80–99%) | 1 sairaudessa |
| ACTG1actin gamma 1 | Usein (30–79%) | 1 sairaudessa |
| ATP1A2ATPase Na+/K+ transporting subunit alpha 2 | Usein (30–79%) | 1 sairaudessa |
| ATP9AATPase phospholipid transporting 9A | Usein (30–79%) | 1 sairaudessa |
| BNIP1BCL2 interacting protein 1 | Usein (30–79%) | 1 sairaudessa |
| CDKL5cyclin dependent kinase like 5 | Usein (30–79%) | 1 sairaudessa |
| CERT1ceramide transporter 1 | Usein (30–79%) | 1 sairaudessa |
| CHASERRCHD2 adjacent suppressive regulatory RNA | Usein (30–79%) | 1 sairaudessa |
| CLPBClpB family mitochondrial disaggregase | Usein (30–79%) | 1 sairaudessa |
| CREBBPCREB binding lysine acetyltransferase | Usein (30–79%) | 1 sairaudessa |
| CTNNA2catenin alpha 2 | Usein (30–79%) | 1 sairaudessa |
| DYRK1Adual specificity tyrosine phosphorylation regulated kinase 1A | Usein (30–79%) | 1 sairaudessa |
| EMC1ER membrane protein complex subunit 1 | Usein (30–79%) | 1 sairaudessa |
| EXOC2exocyst complex component 2 | Usein (30–79%) | 1 sairaudessa |
| FASTKD5FASTK mitochondrial RNA regulator 5 | Usein (30–79%) | 1 sairaudessa |
| GABBR2gamma-aminobutyric acid type B receptor subunit 2 | Usein (30–79%) | 1 sairaudessa |
| GABRB2gamma-aminobutyric acid type A receptor subunit beta2 | Usein (30–79%) | 1 sairaudessa |
| HIVEP2HIVEP zinc finger 2 | Usein (30–79%) | 1 sairaudessa |
| HNRNPH2heterogeneous nuclear ribonucleoprotein H2 | Usein (30–79%) | 1 sairaudessa |
| HNRNPRheterogeneous nuclear ribonucleoprotein R | Usein (30–79%) | 1 sairaudessa |
| INPP4Ainositol polyphosphate-4-phosphatase type I A | Usein (30–79%) | 1 sairaudessa |
| MBD5methyl-CpG binding domain protein 5 | Usein (30–79%) | 1 sairaudessa |
| MECP2methyl-CpG binding protein 2 | Usein (30–79%) | 2 sairaudessa |
| MICOS13mitochondrial contact site and cristae organizing system subunit 13 | Usein (30–79%) | 1 sairaudessa |
| NACC1nucleus accumbens associated 1 | Usein (30–79%) | 1 sairaudessa |
| NDUFA11NADH:ubiquinone oxidoreductase subunit A11 | Usein (30–79%) | 1 sairaudessa |
| NEXMIFneurite extension and migration factor | Usein (30–79%) | 1 sairaudessa |
| NTNG1netrin G1 | Usein (30–79%) | 1 sairaudessa |
| PMPCBpeptidase, mitochondrial processing subunit beta | Usein (30–79%) | 1 sairaudessa |
| RNU5B-1RNA, U5B small nuclear 1 | Usein (30–79%) | 1 sairaudessa |
| SLC1A4solute carrier family 1 member 4 | Usein (30–79%) | 1 sairaudessa |
| SLC25A12solute carrier family 25 member 12 | Usein (30–79%) | 1 sairaudessa |
| SLC39A14solute carrier family 39 member 14 | Usein (30–79%) | 1 sairaudessa |
| SLC9A6solute carrier family 9 member A6 | Usein (30–79%) | 1 sairaudessa |
| SMC1Astructural maintenance of chromosomes 1A | Usein (30–79%) | 1 sairaudessa |
| SMC3structural maintenance of chromosomes 3 | Usein (30–79%) | 1 sairaudessa |
| UBTFupstream binding transcription factor | Usein (30–79%) | 1 sairaudessa |
| UNC13Aunc-13 homolog A | Usein (30–79%) | 1 sairaudessa |
| VPS50VPS50 subunit of EARP/GARPII complex | Usein (30–79%) | 1 sairaudessa |
| WDR37WD repeat domain 37 | Usein (30–79%) | 1 sairaudessa |
| WWOXWW domain containing oxidoreductase | Usein (30–79%) | 1 sairaudessa |
| YRDCyrdC N6-threonylcarbamoyltransferase domain containing | Usein (30–79%) | 1 sairaudessa |
| ZEB2zinc finger E-box binding homeobox 2 | Usein (30–79%) | 2 sairaudessa |
| CHMP1Acharged multivesicular body protein 1A | Joskus (5–29%) | 1 sairaudessa |
| CLTCclathrin heavy chain | Joskus (5–29%) | 1 sairaudessa |
| COG6component of oligomeric golgi complex 6 | Joskus (5–29%) | 1 sairaudessa |
| CRLS1cardiolipin synthase 1 | Joskus (5–29%) | 1 sairaudessa |
| DCXdoublecortin | Joskus (5–29%) | 1 sairaudessa |
| DEGS1delta 4-desaturase, sphingolipid 1 | Joskus (5–29%) | 1 sairaudessa |
| DOLKdolichol kinase | Joskus (5–29%) | 1 sairaudessa |
| GRIN2Aglutamate ionotropic receptor NMDA type subunit 2A | Joskus (5–29%) | 1 sairaudessa |
| IQSEC2IQ motif and Sec7 domain ArfGEF 2 | Joskus (5–29%) | 1 sairaudessa |
| MED16mediator complex subunit 16 | Joskus (5–29%) | 1 sairaudessa |
| NGLY1N-glycanase 1 | Joskus (5–29%) | 1 sairaudessa |
| NTRK2neurotrophic receptor tyrosine kinase 2 | Joskus (5–29%) | 1 sairaudessa |
| PPP1R12Aprotein phosphatase 1 regulatory subunit 12A | Joskus (5–29%) | 1 sairaudessa |
| PRORPprotein only RNase P catalytic subunit | Joskus (5–29%) | 1 sairaudessa |
| PUF60poly(U) binding splicing factor 60 | Joskus (5–29%) | 1 sairaudessa |
| RNU4-2RNA, U4 small nuclear 2 | Joskus (5–29%) | 1 sairaudessa |
| SATB1SATB homeobox 1 | Joskus (5–29%) | 1 sairaudessa |
| SRSF1serine and arginine rich splicing factor 1 | Joskus (5–29%) | 1 sairaudessa |
| TRAPPC12trafficking protein particle complex subunit 12 | Joskus (5–29%) | 1 sairaudessa |
| TRIOtrio Rho guanine nucleotide exchange factor | Joskus (5–29%) | 1 sairaudessa |
| ZRSR2zinc finger CCCH-type, RNA binding motif and serine/arginine rich 2 | Joskus (5–29%) | 1 sairaudessa |
| CARS2cysteinyl-tRNA synthetase 2, mitochondrial | Ei kirjattu | 1 sairaudessa |
| COQ9coenzyme Q9 | Ei kirjattu | 1 sairaudessa |
| DHFRdihydrofolate reductase | Ei kirjattu | 1 sairaudessa |
| DPM2dolichyl-phosphate mannosyltransferase subunit 2, regulatory | Ei kirjattu | 1 sairaudessa |
| HTRA2HtrA serine peptidase 2 | Ei kirjattu | 1 sairaudessa |
| PAFAH1B1platelet activating factor acetylhydrolase 1b regulatory subunit 1 | Ei kirjattu | 1 sairaudessa |
| PLEKHG2pleckstrin homology and RhoGEF domain containing G2 | Ei kirjattu | 1 sairaudessa |
| PPT1palmitoyl-protein thioesterase 1 | Ei kirjattu | 1 sairaudessa |
| PSAT1phosphoserine aminotransferase 1 | Ei kirjattu | 1 sairaudessa |
| RAB3GAP2RAB3 GTPase activating non-catalytic protein subunit 2 | Ei kirjattu | 1 sairaudessa |
| RUSC2RUN and SH3 domain containing 2 | Ei kirjattu | 1 sairaudessa |
| SCN1Asodium voltage-gated channel alpha subunit 1 | Ei kirjattu | 1 sairaudessa |
| SLC12A5solute carrier family 12 member 5 | Ei kirjattu | 1 sairaudessa |
| SLC2A1solute carrier family 2 member 1 | Ei kirjattu | 1 sairaudessa |
| TBC1D24TBC1 domain family member 24 | Ei kirjattu | 1 sairaudessa |
| VPS11VPS11 core subunit of CORVET and HOPS complexes | Ei kirjattu | 1 sairaudessa |
| WDR73WD repeat domain 73 | Ei kirjattu | 1 sairaudessa |
Kuinka usein ilmiö esiintyy ihmisillä, joilla on jokin geenin sairauksista, niin kuin Human Phenotype Ontology sen kirjaa. Nämä sivut kuvaavat piirteitä ja niiden taustalla olevaa tutkimusta, eivätkä ne ole diagnoosi. Oireista kannattaa kysyä lääkäriltä tai geneettiseltä neuvojalta.
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Mistä tämä tieto tulee
- Human Phenotype Ontology, julkaisu 2026-09-01: piirre, sen nimet, määritelmä ja siihen liitetyt geenit. Lue lisää osoitteesta hpo.jax.org.
- Tietojulkaisu 2026.10.19-9814e911.
AtlasKeitä autammeTieteemmeTuotteetTulokset
Kirjaudu sisäänKysySekvensoi genomisi↗
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