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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。
Disproportionate short stature
HP:0003498
對應病歷用詞(4)
- 身材矮小權重 0.8已確認
- short stature權重 0.75已確認
- 矮小權重 0.55待審核
- poor growth權重 0.4待審核
具此 HPO 的疾病（附加參考）(21)
- Achondrogenesis type 1BORPHA:93298 · Very frequent (99-80%)
- AchondroplasiaORPHA:15 · Very frequent (99-80%)
- Autosomal recessive otospondylomegaepiphyseal dysplasiaORPHA:1427 · Very frequent (99-80%)
- Heart defects-limb shortening syndromeORPHA:1354 · Very frequent (99-80%)
- Kniest dysplasiaORPHA:485 · Very frequent (99-80%)
- Kyphomelic dysplasiaORPHA:1801 · Very frequent (99-80%)
- Mesomelic dwarfism, Reinhardt-Pfeiffer typeORPHA:2634 · Very frequent (99-80%)
- Metaphyseal chondrodysplasia, Spahr typeORPHA:2501 · Very frequent (99-80%)
- Microcephalic osteodysplastic primordial dwarfism type IIORPHA:2637 · Very frequent (99-80%)
- Phocomelia, Schinzel typeORPHA:2879 · Very frequent (99-80%)
- Short stature-valvular heart disease-characteristic facies syndromeORPHA:2868 · Very frequent (99-80%)
- Spondylometaphyseal dysplasia, Sedaghatian typeORPHA:93317 · Very frequent (99-80%)
- Acromesomelic dysplasia, Maroteaux typeORPHA:40 · Frequent (79-30%)
- Multiple epiphyseal dysplasia type 4ORPHA:93307 · Frequent (79-30%)
- Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndromeORPHA:508533 · Frequent (79-30%)
- Spondylocarpotarsal synostosisORPHA:3275 · Frequent (79-30%)
- Spondyloepimetaphyseal dysplasia, Missouri typeORPHA:93356 · Frequent (79-30%)
- Spondyloepimetaphyseal dysplasia, Shohat typeORPHA:93352 · Frequent (79-30%)
- Spondyloperipheral dysplasia-short ulna syndromeORPHA:1856 · Frequent (79-30%)
- X-linked hypophosphatemiaORPHA:89936 · Frequent (79-30%)
- Multiple epiphyseal dysplasia type 1ORPHA:93308 · Occasional (29-5%)