# Split fingernails, underdeveloped thumbnails, and triangular lunulae

**Authors:** Erin R. Pomerantz, Nicholas D. Brownstone, Sylvia Hsu

PMC · DOI: 10.1016/j.jdcr.2025.02.009 · 2025-03-07

## Full-text entities

- **Genes:** LMX1B (LIM homeobox transcription factor 1 beta) [NCBI Gene 4010] {aka FSGS10, LMX1.2, NPS1}
- **Diseases:** hypoplasia (MESH:D000080344), onycholysis (MESH:D054039), hypoplastic patellae (MESH:D000092462), Pachyonychia congenita (MESH:D053549), Darier disease (MESH:D007644), Bony abnormalities (MESH:D018213), skeletal abnormalities (MESH:D009139), chronic pulmonary conditions (MESH:D002908), nail abnormalities (MESH:D009264), leukokeratosis (MESH:D007971), COPD (MESH:D029424), bone density loss (MESH:D001851), Osteoporosis (MESH:D010024), radial head dysplasia (MESH:D000092467), Psoriasis (MESH:D011565), Triangular lunulae (OMIM:616827), absent (MESH:D012021), smoking (MESH:D015208), Cardiomyopathy (MESH:D009202), subungual hyperkeratosis (MESH:C535723), absent patellae (MESH:C535568), glaucoma (MESH:D005901), skeletal deformities (MESH:D009140), respiratory dysfunction (MESH:D012131), palmoplantar keratoderma (MESH:D007645), LP (MESH:D008010), inflammatory (MESH:D007249), Nephropathy (MESH:D007674), ocular hypertension (MESH:D009798), end-stage renal disease (MESH:D007676), open-angle glaucoma (MESH:D005902), dorsal pterygium (MESH:D000092142), Fong disease (MESH:D009261), dominant condition (MESH:D020763), Endocrine dysfunction (MESH:D004700), skin condition (MESH:D012871), Renal involvement (MESH:C565423)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12018680/full.md

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Source: https://tomesphere.com/paper/PMC12018680