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以 HPO 交叉檢視
HPO → 對應的病歷用詞，並附加具此 HPO 的疾病作為參考。
Genu varum
HP:0002970
對應病歷用詞(3)
- 膝內翻權重 0.9已確認
- 型腿權重 0.85已確認
- bow-leggedness權重 0.7待審核
具此 HPO 的疾病（附加參考）(39)
- Autosomal recessive hypophosphatemic ricketsORPHA:289176 · Very frequent (99-80%)
- Epiphyseal stippling-osteoclastic hyperplasia syndromeORPHA:1952 · Very frequent (99-80%)
- Facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndromeORPHA:1969 · Very frequent (99-80%)
- Hypocalcemic vitamin D-dependent ricketsORPHA:289157 · Very frequent (99-80%)
- Léri-Weill dyschondrosteosisORPHA:240 · Very frequent (99-80%)
- Metaphyseal chondrodysplasia, Spahr typeORPHA:2501 · Very frequent (99-80%)
- Orofaciodigital syndrome type 4ORPHA:2753 · Very frequent (99-80%)
- Satoyoshi syndromeORPHA:3130 · Very frequent (99-80%)
- Acrocapitofemoral dysplasiaORPHA:63446 · Frequent (79-30%)
- AcrodysostosisORPHA:950 · Frequent (79-30%)
- Dysplasia epiphysealis hemimelicaORPHA:1822 · Frequent (79-30%)
- Hypocalcemic vitamin D-resistant ricketsORPHA:93160 · Frequent (79-30%)
- HypochondroplasiaORPHA:429 · Frequent (79-30%)
- Megalocornea-intellectual disability syndromeORPHA:2479 · Frequent (79-30%)
- Metaphyseal chondrodysplasia, Schmid typeORPHA:174 · Frequent (79-30%)
- Metaphyseal dysostosis-intellectual disability-conductive deafness syndromeORPHA:2502 · Frequent (79-30%)
- Multiple epiphyseal dysplasia type 5ORPHA:93311 · Frequent (79-30%)
- Platyspondylic dysplasia, Torrance typeORPHA:85166 · Frequent (79-30%)
- Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic typeORPHA:93360 · Frequent (79-30%)
- Spondyloepimetaphyseal dysplasia, Missouri typeORPHA:93356 · Frequent (79-30%)
- Spondylometaphyseal dysplasia, 'corner fracture' typeORPHA:93315 · Frequent (79-30%)
- Spondylometaphyseal dysplasia, Kozlowski typeORPHA:93314 · Frequent (79-30%)
- Temtamy syndromeORPHA:1777 · Frequent (79-30%)
- Thrombocytopenia-absent radius syndromeORPHA:3320 · Frequent (79-30%)
- X-linked hypophosphatemiaORPHA:89936 · Frequent (79-30%)
- Aortic arch anomaly-facial dysmorphism-intellectual disability syndromeORPHA:1110 · Occasional (29-5%)
- Mesomelic dysplasia, Nievergelt typeORPHA:2633 · Occasional (29-5%)
- Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduriaORPHA:99646 · Occasional (29-5%)
- Multiple epiphyseal dysplasia due to collagen 9 anomalyORPHA:166002 · Occasional (29-5%)
- Neurofibromatosis type 1ORPHA:636 · Occasional (29-5%)
- Ollier diseaseORPHA:296 · Occasional (29-5%)
- PachydermoperiostosisORPHA:2796 · Occasional (29-5%)
- Progressive pseudorheumatoid dysplasiaORPHA:1159 · Occasional (29-5%)
- PseudoachondroplasiaORPHA:750 · Occasional (29-5%)
- Rothmund-Thomson syndrome type 2ORPHA:221016 · Occasional (29-5%)
- Spondyloepimetaphyseal dysplasia, Shohat typeORPHA:93352 · Occasional (29-5%)
- Typical nemaline myopathyORPHA:171436 · Occasional (29-5%)
- Multiple epiphyseal dysplasia type 1ORPHA:93308 · Very rare (<4-1%)
- Rothmund-Thomson syndrome type 1ORPHA:221008 · Very rare (<4-1%)