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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。
Delayed ability to walk
HP:0031936
對應病歷用詞(2)
- late walker權重 0.65待審核
- delayed walking權重 0.6待審核
具此 HPO 的疾病（附加參考）(38)
- 3-methylglutaconic aciduria type 9ORPHA:505216 · Very frequent (99-80%)
- Arthrochalasia Ehlers-Danlos syndromeORPHA:1899 · Very frequent (99-80%)
- Autosomal recessive cerebelloparenchymal disorder type 3ORPHA:1170 · Very frequent (99-80%)
- Bilateral generalized polymicrogyriaORPHA:208447 · Very frequent (99-80%)
- CNTNAP2-related developmental and epileptic encephalopathyORPHA:163681 · Very frequent (99-80%)
- Houge-Janssens syndrome type 1ORPHA:457279 · Very frequent (99-80%)
- Lamb-Shaffer syndromeORPHA:530983 · Very frequent (99-80%)
- Pelizaeus-Merzbacher disease, classic formORPHA:280219 · Very frequent (99-80%)
- PMP22-RAI1 contiguous gene duplication syndromeORPHA:477817 · Very frequent (99-80%)
- X-linked sideroblastic anemia and spinocerebellar ataxiaORPHA:2802 · Very frequent (99-80%)
- AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndromeORPHA:412069 · Frequent (79-30%)
- Allan-Herndon-Dudley syndromeORPHA:59 · Frequent (79-30%)
- Angelman syndrome due to imprinting defect in 15q11-q13ORPHA:411515 · Frequent (79-30%)
- Bartter syndrome type 4ORPHA:89938 · Frequent (79-30%)
- Early-onset epilepsy-intellectual disability-brain anomalies syndromeORPHA:488635 · Frequent (79-30%)
- FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndromeORPHA:404451 · Frequent (79-30%)
- Gabriele-de Vries syndromeORPHA:506358 · Frequent (79-30%)
- Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndromeORPHA:2269 · Frequent (79-30%)
- Intellectual disability-seizures-abnormal gait-facial dysmorphism syndromeORPHA:513456 · Frequent (79-30%)
- Juvenile amyotrophic lateral sclerosisORPHA:300605 · Frequent (79-30%)
- Macrocephaly-developmental delay syndromeORPHA:397612 · Frequent (79-30%)
- Mowat-Wilson syndromeORPHA:2152 · Frequent (79-30%)
- Mowat-Wilson syndrome due to a ZEB2 point mutationORPHA:261552 · Frequent (79-30%)
- Mowat-Wilson syndrome due to monosomy 2q22ORPHA:261537 · Frequent (79-30%)
- Muscle-eye-brain disease with bilateral multicystic leucodystrophyORPHA:370997 · Frequent (79-30%)
- Myopathic Ehlers-Danlos syndromeORPHA:536516 · Frequent (79-30%)
- Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletionORPHA:352665 · Frequent (79-30%)
- Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutationORPHA:453504 · Frequent (79-30%)
- Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndromeORPHA:477993 · Frequent (79-30%)
- Pyruvate dehydrogenase E2 deficiencyORPHA:79244 · Frequent (79-30%)
- Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndromeORPHA:480864 · Frequent (79-30%)
- X-linked Charcot-Marie-Tooth disease type 3ORPHA:101077 · Frequent (79-30%)
- X-linked hypophosphatemiaORPHA:89936 · Frequent (79-30%)
- Alström syndromeORPHA:64 · Occasional (29-5%)
- DK1-CDGORPHA:91131 · Occasional (29-5%)
- Imerslund-Gräsbeck syndromeORPHA:35858 · Occasional (29-5%)
- Opitz GBBB syndromeORPHA:2745 · Occasional (29-5%)
- Usher syndromeORPHA:886 · Occasional (29-5%)