Trait
Abnormalities of the fingers
Clinical name: Abnormal finger morphology
An anomaly of a finger.
Summary
- Also called
- Abnormality of finger
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test22 genes linked to Abnormalities of the fingers
Changes in these genes cause rare conditions in which Abnormalities of the fingers 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 |
|---|---|---|
| AKT1AKT serine/threonine kinase 1 | Very often (80–99%) | In 1 condition |
| ATP6V1B2ATPase H+ transporting V1 subunit B2 | Very often (80–99%) | In 1 condition |
| PAX3paired box 3 | Very often (80–99%) | In 1 condition |
| RNU4ATACRNA, U4atac small nuclear | Very often (80–99%) | In 1 condition |
| TBC1D24TBC1 domain family member 24 | Very often (80–99%) | In 1 condition |
| TBX3T-box transcription factor 3 | Very often (80–99%) | In 1 condition |
| ADNPactivity dependent neuroprotector homeobox | Often (30–79%) | In 1 condition |
| ATP13A2ATPase cation transporting 13A2 | Often (30–79%) | In 1 condition |
| COG7component of oligomeric golgi complex 7 | Often (30–79%) | In 1 condition |
| CYP27A1cytochrome P450 family 27 subfamily A member 1 | Often (30–79%) | In 1 condition |
| ESCO2establishment of sister chromatid cohesion N-acetyltransferase 2 | Often (30–79%) | In 1 condition |
| FIG4FIG4 phosphoinositide 5-phosphatase | Often (30–79%) | In 1 condition |
| PTDSS1phosphatidylserine synthase 1 | Often (30–79%) | In 1 condition |
| SIL1SIL1 nucleotide exchange factor | Often (30–79%) | In 1 condition |
| SMARCA2SWI/SNF related BAF chromatin remodeling complex subunit ATPase 2 | Often (30–79%) | In 1 condition |
| VAC14VAC14 component of PIKFYVE complex | Often (30–79%) | In 1 condition |
| DNAJC21DnaJ heat shock protein family (Hsp40) member C21 | Rarely (1–4%) | In 1 condition |
| EFL1elongation factor like GTPase 1 | Rarely (1–4%) | In 1 condition |
| SBDSSBDS ribosome maturation factor | Rarely (1–4%) | In 1 condition |
| HRASHRas proto-oncogene, GTPase | Not recorded | In 1 condition |
| KRASKRas proto-oncogene, GTPase | Not recorded | In 1 condition |
| NRASNRAS proto-oncogene, GTPase | Not recorded | 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
- Long fingers72 genes
- Abnormality of the thumb41 genes
- Slender finger36 genes
- Broad finger32 genes
- Absent/small fingers24 genes
- Increased mobility in finger joint19 genes
- Swan neck-like deformities of the fingers10 genes
- Finger joint contracture8 genes
- Atypical position of finger7 genes
- Abnormality of the fingertips6 genes
- Finger swelling5 genes
- Abnormal finger flexion crease3 genes
- Trident hand3 genes
- Mallet finger2 genes
- Curved fingers1 gene
- Sausage fingers1 gene
- Spindle-shaped finger1 gene
- Abnormal 3rd finger morphology
- Abnormal 4th finger morphology
- Abnormality of index finger
- Abnormality of the finger bones
- Abnormality of the little finger
Broader traits
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 2026.10.16-c6eea6bf.
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