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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 valgum
HP:0002857
對應病歷用詞(1)
- knock knees權重 0.85已確認
具此 HPO 的疾病（附加參考）(98)
- HIDEA syndromeORPHA:436141 · Obligate (100%)
- Aromatase deficiencyORPHA:91 · Very frequent (99-80%)
- Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndromeORPHA:436174 · Very frequent (99-80%)
- CHST3-related skeletal dysplasiaORPHA:263463 · Very frequent (99-80%)
- Difference of sex development-intellectual disability syndromeORPHA:2983 · Very frequent (99-80%)
- Dysmorphism-pectus carinatum-joint laxity syndromeORPHA:2104 · Very frequent (99-80%)
- Ellis-Van Creveld syndromeORPHA:289 · Very frequent (99-80%)
- Facial dysmorphism-shawl scrotum-joint laxity syndromeORPHA:1778 · Very frequent (99-80%)
- Mesomelic dysplasia, Nievergelt typeORPHA:2633 · Very frequent (99-80%)
- Microtriplication 11q24.1 syndromeORPHA:289522 · Very frequent (99-80%)
- Mucopolysaccharidosis type 4ORPHA:582 · Very frequent (99-80%)
- Multiple epiphyseal dysplasia-macrocephaly-facial dysmorphism syndromeORPHA:166024 · Very frequent (99-80%)
- Multiple epiphyseal dysplasia, Lowry typeORPHA:166016 · Very frequent (99-80%)
- Non-eruption of teeth-maxillary hypoplasia-genu valgum syndromeORPHA:2972 · Very frequent (99-80%)
- Pseudoleprechaunism syndrome, Patterson typeORPHA:2976 · Very frequent (99-80%)
- Pyle diseaseORPHA:3005 · Very frequent (99-80%)
- Rhizomelic dysplasia, Patterson-Lowry typeORPHA:2831 · Very frequent (99-80%)
- Schwartz-Jampel syndromeORPHA:800 · Very frequent (99-80%)
- SHOX-related short statureORPHA:314795 · Very frequent (99-80%)
- Spondyloepimetaphyseal dysplasia, Irapa typeORPHA:93351 · Very frequent (99-80%)
- Thoracomelic dysplasiaORPHA:1803 · Very frequent (99-80%)
- X-linked intellectual disability, Stevenson typeORPHA:85325 · Very frequent (99-80%)
- Acrocraniofacial dysostosisORPHA:949 · Frequent (79-30%)
- Albers-Schönberg osteopetrosisORPHA:53 · Frequent (79-30%)
- Atelosteogenesis type IIORPHA:56304 · Frequent (79-30%)
- Beta-mercaptolactate cysteine disulfiduriaORPHA:1035 · Frequent (79-30%)
- Beta-thalassemia majorORPHA:231214 · Frequent (79-30%)
- Brachytelephalangy-dysmorphism-Kallmann syndromeORPHA:1295 · Frequent (79-30%)
- Cardiac-valvular Ehlers-Danlos syndromeORPHA:230851 · Frequent (79-30%)
- Carpenter syndromeORPHA:65759 · Frequent (79-30%)
- Cohen syndromeORPHA:193 · Frequent (79-30%)
- Congenital patella dislocationORPHA:295036 · Frequent (79-30%)
- Diastrophic dysplasiaORPHA:628 · Frequent (79-30%)
- Distal deletion 15q syndromeORPHA:1596 · Frequent (79-30%)
- Distal duplication 17q syndromeORPHA:3379 · Frequent (79-30%)
- Dysplasia epiphysealis hemimelicaORPHA:1822 · Frequent (79-30%)
- DysspondyloenchondromatosisORPHA:85198 · Frequent (79-30%)
- Homocystinuria due to cystathionine beta-synthase deficiencyORPHA:394 · Frequent (79-30%)
- Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndromeORPHA:293967 · Frequent (79-30%)
- Isolated fibular hemimeliaORPHA:93323 · Frequent (79-30%)
- Isolated megalencephalyORPHA:2477 · Frequent (79-30%)
- Léri-Weill dyschondrosteosisORPHA:240 · Frequent (79-30%)
- Marshall syndromeORPHA:560 · Frequent (79-30%)
- Monosomy X syndromeORPHA:99226 · Frequent (79-30%)
- Mosaic monosomy X syndromeORPHA:99228 · Frequent (79-30%)
- Mowat-Wilson syndromeORPHA:2152 · Frequent (79-30%)
- Mucolipidosis type IIIORPHA:577 · Frequent (79-30%)
- Mucopolysaccharidosis type 3ORPHA:581 · Frequent (79-30%)
- Mucopolysaccharidosis type 6ORPHA:583 · Frequent (79-30%)
- Multiple epiphyseal dysplasia type 4ORPHA:93307 · Frequent (79-30%)
- Multiple epiphyseal dysplasia type 5ORPHA:93311 · Frequent (79-30%)
- Neurofibromatosis type 1ORPHA:636 · Frequent (79-30%)
- Osteogenesis imperfectaORPHA:666 · Frequent (79-30%)
- Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndromeORPHA:457395 · Frequent (79-30%)
- Prolidase deficiencyORPHA:742 · Frequent (79-30%)
- SPONASTRIME dysplasiaORPHA:93357 · Frequent (79-30%)
- Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic typeORPHA:93360 · Frequent (79-30%)
- Spondyloepiphyseal dysplasia congenitaORPHA:94068 · Frequent (79-30%)
- Spondylometaphyseal dysplasia, 'corner fracture' typeORPHA:93315 · Frequent (79-30%)
- Spondylometaphyseal dysplasia, Schmidt typeORPHA:93316 · Frequent (79-30%)
- Stickler syndromeORPHA:828 · Frequent (79-30%)
- Stüve-Wiedemann syndromeORPHA:3206 · Frequent (79-30%)
- Turner syndromeORPHA:881 · Frequent (79-30%)
- Turner syndrome due to structural X chromosome anomaliesORPHA:99413 · Frequent (79-30%)
- Williams syndromeORPHA:904 · Frequent (79-30%)
- X-linked hypophosphatemiaORPHA:89936 · Frequent (79-30%)
- Alpha-mannosidosis, infantile formORPHA:309282 · Occasional (29-5%)
- Autosomal recessive spastic paraplegia type 20ORPHA:101000 · Occasional (29-5%)
- Camurati-Engelmann diseaseORPHA:1328 · Occasional (29-5%)
- Cardiofaciocutaneous syndromeORPHA:1340 · Occasional (29-5%)
- Cleidocranial dysplasiaORPHA:1452 · Occasional (29-5%)
- COG5-CDGORPHA:263487 · Occasional (29-5%)
- Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutationORPHA:300570 · Occasional (29-5%)
- Dyggve-Melchior-Clausen diseaseORPHA:239 · Occasional (29-5%)
- Giant axonal neuropathyORPHA:643 · Occasional (29-5%)
- Hypocalcemic vitamin D-resistant ricketsORPHA:93160 · Occasional (29-5%)
- Mesomelia-synostoses syndromeORPHA:2496 · Occasional (29-5%)
- Mowat-Wilson syndrome due to a ZEB2 point mutationORPHA:261552 · Occasional (29-5%)
- Mowat-Wilson syndrome due to monosomy 2q22ORPHA:261537 · Occasional (29-5%)
- Multiple epiphyseal dysplasia due to collagen 9 anomalyORPHA:166002 · Occasional (29-5%)
- Multiple osteochondromasORPHA:321 · Occasional (29-5%)
- Neurofibromatosis type 1 due to NF1 mutation or intragenic deletionORPHA:363700 · Occasional (29-5%)
- Non-acquired isolated growth hormone deficiencyORPHA:631 · Occasional (29-5%)
- Occipital horn syndromeORPHA:198 · Occasional (29-5%)
- Oculocerebrorenal syndrome of LoweORPHA:534 · Occasional (29-5%)
- Oculofaciocardiodental syndromeORPHA:2712 · Occasional (29-5%)
- Ollier diseaseORPHA:296 · Occasional (29-5%)
- Progressive pseudorheumatoid dysplasiaORPHA:1159 · Occasional (29-5%)
- PseudoachondroplasiaORPHA:750 · Occasional (29-5%)
- Richieri Costa-da Silva syndromeORPHA:3101 · Occasional (29-5%)
- Ring chromosome 7 syndromeORPHA:1449 · Occasional (29-5%)
- Roussy-Lévy syndromeORPHA:3115 · Occasional (29-5%)
- Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndromeORPHA:488627 · Occasional (29-5%)
- Shprintzen-Goldberg syndromeORPHA:2462 · Occasional (29-5%)
- Trichorhinophalangeal syndrome type 2ORPHA:502 · Occasional (29-5%)
- Typical nemaline myopathyORPHA:171436 · Occasional (29-5%)
- Unstable beta globin chain variant diseaseORPHA:231226 · Occasional (29-5%)
- Multiple epiphyseal dysplasia type 1ORPHA:93308 · Very rare (<4-1%)