Trait

Abnormal intervertebral disk morphology

Any structural abnormality of the intervertebral disk.

Also called: Abnormality of the intervertebral disc, Abnormality of the intervertebral disk
Body system: Abnormality of the musculoskeletal system

This page as data

Add .json to the page's address, or ask for application/json, to read it as JSON.

library(jsonlite)

url <- "https://dantelabs.com/traits/abnormal-intervertebral-disk-morphology.json"
page <- fromJSON(url)
page$trait$name

Open the JSON

Read the genes linked to Abnormal intervertebral disk morphology, and the rest of your genome, with one test.

From $449Free shipping · Results in 6–8 weeks

Get my Genome Test

24 genes linked to Abnormal intervertebral disk morphology

Changes in these genes cause rare conditions in which Abnormal intervertebral disk morphology is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.

Gene	How often it is seen	Conditions
ANKHANKH inorganic pyrophosphate transport regulator	Very often (80–99%)	In 1 condition
DLL3delta like canonical Notch ligand 3	Very often (80–99%)	In 1 condition
HES7hes family bHLH transcription factor 7	Very often (80–99%)	In 1 condition
LFNGLFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	Very often (80–99%)	In 1 condition
MESP2mesoderm posterior bHLH transcription factor 2	Very often (80–99%)	In 1 condition
RIPPLY2ripply transcriptional repressor 2	Very often (80–99%)	In 1 condition
RNU4ATACRNA, U4atac small nuclear	Very often (80–99%)	In 1 condition
TBX6T-box transcription factor 6	Very often (80–99%)	In 1 condition
TNFRSF11BTNF receptor superfamily member 11b	Very often (80–99%)	In 1 condition
TRPV4transient receptor potential cation channel subfamily V member 4	Very often (80–99%)	In 1 condition
XYLT2xylosyltransferase 2	Very often (80–99%)	In 1 condition
GON7GON7 subunit of KEOPS complex	Sometimes (5–29%)	In 1 condition
HOXD13homeobox D13	Sometimes (5–29%)	In 1 condition
LAGE3L antigen family member 3	Sometimes (5–29%)	In 1 condition
NUP107nucleoporin 107	Sometimes (5–29%)	In 1 condition
NUP133nucleoporin 133	Sometimes (5–29%)	In 1 condition
OSGEPO-sialoglycoprotein endopeptidase	Sometimes (5–29%)	In 1 condition
PPP1CBprotein phosphatase 1 catalytic subunit beta	Sometimes (5–29%)	In 1 condition
SHOC2SHOC2 leucine rich repeat scaffold protein	Sometimes (5–29%)	In 1 condition
TP53RKTP53 regulating kinase	Sometimes (5–29%)	In 1 condition
TPRKBTP53RK binding protein	Sometimes (5–29%)	In 1 condition
WDR4WDR4 tRNA N7-guanosine methyltransferase non-catalytic subunit	Sometimes (5–29%)	In 1 condition
WDR73WD repeat domain 73	Sometimes (5–29%)	In 1 condition
YRDCyrdC N6-threonylcarbamoyltransferase domain containing	Sometimes (5–29%)	In 1 condition

How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.

Narrower traits

Broader traits

Abnormality of the vertebral column

Where this comes from

The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
Data release 2026.10.17-8666dff2.

One test. A lifetime of answers.