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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。
Spinal canal stenosis
HP:0003416
對應病歷用詞(0)
尚無對應用詞。
具此 HPO 的疾病（附加參考）(24)
- Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndromeORPHA:436174 · Very frequent (99-80%)
- AchondroplasiaORPHA:15 · Frequent (79-30%)
- AcrodysostosisORPHA:950 · Frequent (79-30%)
- AcromegalyORPHA:963 · Frequent (79-30%)
- Autosomal recessive hypophosphatemic ricketsORPHA:289176 · Frequent (79-30%)
- Epidermal nevus syndromeORPHA:35125 · Frequent (79-30%)
- Hurler-Scheie syndromeORPHA:93476 · Frequent (79-30%)
- Mucopolysaccharidosis type 4ORPHA:582 · Frequent (79-30%)
- SomatomammotropinomaORPHA:314769 · Frequent (79-30%)
- 1p36 deletion syndromeORPHA:1606 · Occasional (29-5%)
- AL amyloidosisORPHA:85443 · Occasional (29-5%)
- ATTRV122I amyloidosisORPHA:85451 · Occasional (29-5%)
- Brachytelephalangic chondrodysplasia punctataORPHA:79345 · Occasional (29-5%)
- Hurler syndromeORPHA:93473 · Occasional (29-5%)
- HypochondroplasiaORPHA:429 · Occasional (29-5%)
- Isolated Klippel-Feil syndromeORPHA:2345 · Occasional (29-5%)
- Mosaic trisomy 20 syndromeORPHA:1724 · Occasional (29-5%)
- Mucopolysaccharidosis type 1ORPHA:579 · Occasional (29-5%)
- NeurofibromaORPHA:252183 · Occasional (29-5%)
- Sanjad-Sakati syndromeORPHA:2323 · Occasional (29-5%)
- Stickler syndromeORPHA:828 · Occasional (29-5%)
- Wild type ATTR amyloidosisORPHA:330001 · Occasional (29-5%)
- X-linked hypophosphatemiaORPHA:89936 · Occasional (29-5%)
- Idiopathic camptocormiaORPHA:1320 · Very rare (<4-1%)