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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。
Tinnitus
HP:0000360
對應病歷用詞(0)
尚無對應用詞。
具此 HPO 的疾病（附加參考）(35)
- ArachnoiditisORPHA:137817 · Very frequent (99-80%)
- Cogan syndromeORPHA:1467 · Very frequent (99-80%)
- Polycythemia veraORPHA:729 · Very frequent (99-80%)
- Alpha-N-acetylgalactosaminidase deficiency type 2ORPHA:79280 · Frequent (79-30%)
- Arnold-Chiari malformation type IORPHA:268882 · Frequent (79-30%)
- Carney-Stratakis syndromeORPHA:97286 · Frequent (79-30%)
- Episodic ataxia type 3ORPHA:79135 · Frequent (79-30%)
- Fabry diseaseORPHA:324 · Frequent (79-30%)
- Familial paroxysmal ataxiaORPHA:97 · Frequent (79-30%)
- Relapsing polychondritisORPHA:728 · Frequent (79-30%)
- Visual snow syndromeORPHA:420556 · Frequent (79-30%)
- Vogt-Koyanagi-Harada diseaseORPHA:3437 · Frequent (79-30%)
- Adrenocortical carcinoma with pure aldosterone hypersecretionORPHA:231625 · Occasional (29-5%)
- Central neurocytomaORPHA:73256 · Occasional (29-5%)
- Charcot-Marie-Tooth disease type 1EORPHA:90658 · Occasional (29-5%)
- Ectopic aldosterone-producing tumorORPHA:231632 · Occasional (29-5%)
- Episodic ataxia type 7ORPHA:209970 · Occasional (29-5%)
- Familial hyperaldosteronism type IORPHA:403 · Occasional (29-5%)
- Familial hyperaldosteronism type IIORPHA:404 · Occasional (29-5%)
- Familial hyperaldosteronism type IIIORPHA:251274 · Occasional (29-5%)
- Familial or sporadic hemiplegic migraineORPHA:569 · Occasional (29-5%)
- Full NF2-related schwannomatosisORPHA:637 · Occasional (29-5%)
- Full schwannomatosisORPHA:93921 · Occasional (29-5%)
- Madras motor neuron diseaseORPHA:137867 · Occasional (29-5%)
- Middle ear neuroendocrine tumorORPHA:100084 · Occasional (29-5%)
- Primary hyperaldosteronism-seizures-neurological abnormalities syndromeORPHA:369929 · Occasional (29-5%)
- Primary unilateral adrenal hyperplasiaORPHA:231580 · Occasional (29-5%)
- Susac syndromeORPHA:838 · Occasional (29-5%)
- Sympathetic ophthalmiaORPHA:79098 · Occasional (29-5%)
- Tick-borne encephalitisORPHA:297 · Occasional (29-5%)
- TrichinellosisORPHA:863 · Occasional (29-5%)
- Usher syndromeORPHA:886 · Occasional (29-5%)
- X-linked hypophosphatemiaORPHA:89936 · Occasional (29-5%)
- Gitelman syndromeORPHA:358 · Very rare (<4-1%)
- MeningiomaORPHA:2495 · Very rare (<4-1%)