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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。
Bowing of the long bones
HP:0006487
對應病歷用詞(0)
尚無對應用詞。
具此 HPO 的疾病（附加參考）(63)
- Acromesomelic dysplasia, Grebe typeORPHA:2098 · Very frequent (99-80%)
- Autosomal recessive malignant osteopetrosisORPHA:667 · Very frequent (99-80%)
- B3GALT6-related spondylodysplastic Ehlers-Danlos syndromeORPHA:536467 · Very frequent (99-80%)
- Campomelia, Cumming typeORPHA:1318 · Very frequent (99-80%)
- Campomelic dysplasiaORPHA:140 · Very frequent (99-80%)
- Cartilage-hair hypoplasiaORPHA:175 · Very frequent (99-80%)
- Cloverleaf skull-multiple congenital anomalies syndromeORPHA:93267 · Very frequent (99-80%)
- Cole-Carpenter syndromeORPHA:2050 · Very frequent (99-80%)
- Craniofacial dysostosis-diaphyseal hyperplasia syndromeORPHA:1798 · Very frequent (99-80%)
- Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndromeORPHA:171839 · Very frequent (99-80%)
- Diastrophic dysplasiaORPHA:628 · Very frequent (99-80%)
- Epiphyseal stippling-osteoclastic hyperplasia syndromeORPHA:1952 · Very frequent (99-80%)
- Ghosal hematodiaphyseal dysplasiaORPHA:1802 · Very frequent (99-80%)
- Gnathodiaphyseal dysplasiaORPHA:53697 · Very frequent (99-80%)
- Grant syndromeORPHA:2097 · Very frequent (99-80%)
- Growth delay-hydrocephaly-lung hypoplasia syndromeORPHA:3035 · Very frequent (99-80%)
- Juvenile Paget diseaseORPHA:2801 · Very frequent (99-80%)
- Kyphomelic dysplasiaORPHA:1801 · Very frequent (99-80%)
- Langer mesomelic dysplasiaORPHA:2632 · Very frequent (99-80%)
- Marshall-Smith syndromeORPHA:561 · Very frequent (99-80%)
- Melnick-Needles syndromeORPHA:2484 · Very frequent (99-80%)
- Mesomelic dwarfism-cleft palate-camptodactyly syndromeORPHA:2631 · Very frequent (99-80%)
- Mesomelic dysplasia, Savarirayan typeORPHA:85170 · Very frequent (99-80%)
- Metaphyseal anadysplasiaORPHA:1040 · Very frequent (99-80%)
- Metaphyseal chondrodysplasia, Spahr typeORPHA:2501 · Very frequent (99-80%)
- Mucopolysaccharidosis type 4ORPHA:582 · Very frequent (99-80%)
- Otopalatodigital syndrome type 2ORPHA:90652 · Very frequent (99-80%)
- Phocomelia, Schinzel typeORPHA:2879 · Very frequent (99-80%)
- Platyspondylic dysplasia, Torrance typeORPHA:85166 · Very frequent (99-80%)
- Roberts syndromeORPHA:3103 · Very frequent (99-80%)
- Schwartz-Jampel syndromeORPHA:800 · Very frequent (99-80%)
- Spondylometaphyseal dysplasia-cone-rod dystrophy syndromeORPHA:85167 · Very frequent (99-80%)
- Stüve-Wiedemann syndromeORPHA:3206 · Very frequent (99-80%)
- Thanatophoric dysplasia type 1ORPHA:1860 · Very frequent (99-80%)
- Weismann-Netter syndromeORPHA:3344 · Very frequent (99-80%)
- AcrodysostosisORPHA:950 · Frequent (79-30%)
- Acromesomelic dysplasia, Maroteaux typeORPHA:40 · Frequent (79-30%)
- Alpha-mannosidosisORPHA:61 · Frequent (79-30%)
- Baller-Gerold syndromeORPHA:1225 · Frequent (79-30%)
- Beta-thalassemia majorORPHA:231214 · Frequent (79-30%)
- Blomstrand lethal chondrodysplasiaORPHA:50945 · Frequent (79-30%)
- Fibrous dysplasia of boneORPHA:249 · Frequent (79-30%)
- Metaphyseal chondrodysplasia, Jansen typeORPHA:33067 · Frequent (79-30%)
- Oncogenic osteomalaciaORPHA:352540 · Frequent (79-30%)
- Otopalatodigital syndrome type 1ORPHA:90650 · Frequent (79-30%)
- Van den Ende-Gupta syndromeORPHA:2460 · Frequent (79-30%)
- X-linked hypophosphatemiaORPHA:89936 · Frequent (79-30%)
- Bruck syndromeORPHA:2771 · Occasional (29-5%)
- Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiencyORPHA:95699 · Occasional (29-5%)
- Distal 22q11.2 microdeletion syndromeORPHA:261330 · Occasional (29-5%)
- Fanconi-Bickel syndromeORPHA:2088 · Occasional (29-5%)
- Hajdu-Cheney syndromeORPHA:955 · Occasional (29-5%)
- HypochondroplasiaORPHA:429 · Occasional (29-5%)
- HypophosphatasiaORPHA:436 · Occasional (29-5%)
- Meckel syndromeORPHA:564 · Occasional (29-5%)
- Menkes diseaseORPHA:565 · Occasional (29-5%)
- Microphthalmia with limb anomaliesORPHA:1106 · Occasional (29-5%)
- Multiple osteochondromasORPHA:321 · Occasional (29-5%)
- OdontochondrodysplasiaORPHA:166272 · Occasional (29-5%)
- Osteogenesis imperfectaORPHA:666 · Occasional (29-5%)
- Shprintzen-Goldberg syndromeORPHA:2462 · Occasional (29-5%)
- Spondylodysplastic Ehlers-Danlos syndromeORPHA:536471 · Occasional (29-5%)
- Unstable beta globin chain variant diseaseORPHA:231226 · Occasional (29-5%)