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HPO → 對應的病歷用詞，並附加具此 HPO 的疾病作為參考。
Spinal cord compression
HP:0002176
對應病歷用詞(0)
尚無對應用詞。
具此 HPO 的疾病（附加參考）(22)
- Craniofacial conodysplasiaORPHA:85168 · Very frequent (99-80%)
- Microcephaly-cervical spine fusion anomalies syndromeORPHA:2522 · Very frequent (99-80%)
- Epidermal nevus syndromeORPHA:35125 · Frequent (79-30%)
- Diastrophic dysplasiaORPHA:628 · Occasional (29-5%)
- Familial papillary or follicular thyroid carcinomaORPHA:319487 · Occasional (29-5%)
- Gaucher disease type 1ORPHA:77259 · Occasional (29-5%)
- IgG4-related pachymeningitisORPHA:449427 · Occasional (29-5%)
- Large/giant congenital melanocytic nevusORPHA:626 · Occasional (29-5%)
- Mucolipidosis type IIIORPHA:577 · Occasional (29-5%)
- Mucopolysaccharidosis type 2ORPHA:580 · Occasional (29-5%)
- Multiple myelomaORPHA:29073 · Occasional (29-5%)
- NeuroblastomaORPHA:635 · Occasional (29-5%)
- Neurocutaneous melanocytosisORPHA:2481 · Occasional (29-5%)
- Pseudohypoparathyroidism type 1AORPHA:79443 · Occasional (29-5%)
- Spondyloepimetaphyseal dysplasia congenita, Strudwick typeORPHA:93346 · Occasional (29-5%)
- Spondyloepiphyseal dysplasia congenitaORPHA:94068 · Occasional (29-5%)
- Variant ABeta2M amyloidosisORPHA:314652 · Occasional (29-5%)
- X-linked hypophosphatemiaORPHA:89936 · Occasional (29-5%)
- Beta-thalassemia intermediaORPHA:231222 · Very rare (<4-1%)
- Gorham-Stout diseaseORPHA:73 · Very rare (<4-1%)
- Kniest dysplasiaORPHA:485 · Very rare (<4-1%)
- Multiple osteochondromasORPHA:321 · Very rare (<4-1%)