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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。
Cellulitis
HP:0100658
對應病歷用詞(0)
尚無對應用詞。
具此 HPO 的疾病（附加參考）(34)
- Caffey diseaseORPHA:1310 · Very frequent (99-80%)
- CalciphylaxisORPHA:280062 · Very frequent (99-80%)
- Dissecting cellulitis of the scalpORPHA:345 · Very frequent (99-80%)
- Eosinophilic fasciitisORPHA:3165 · Very frequent (99-80%)
- SLC35A1-CDGORPHA:238459 · Very frequent (99-80%)
- Wells syndromeORPHA:901 · Very frequent (99-80%)
- Anal fistulaORPHA:228113 · Frequent (79-30%)
- Capillary-lymphatic-venous malformation with segmental distributionORPHA:90308 · Frequent (79-30%)
- DracunculiasisORPHA:231 · Frequent (79-30%)
- Meige diseaseORPHA:90186 · Frequent (79-30%)
- Milroy diseaseORPHA:79452 · Frequent (79-30%)
- X-linked agammaglobulinemiaORPHA:47 · Frequent (79-30%)
- Autosomal dominant hyper-IgE syndrome due to STAT3 deficiencyORPHA:2314 · Occasional (29-5%)
- Autosomal dominant severe congenital neutropeniaORPHA:486 · Occasional (29-5%)
- Autosomal non-syndromic agammaglobulinemiaORPHA:33110 · Occasional (29-5%)
- Bacterial toxic-shock syndromeORPHA:36234 · Occasional (29-5%)
- Classical-like Ehlers-Danlos syndrome type 2ORPHA:536532 · Occasional (29-5%)
- Cyclic neutropeniaORPHA:2686 · Occasional (29-5%)
- Familial partial lipodystrophy, Dunnigan typeORPHA:2348 · Occasional (29-5%)
- Felty syndromeORPHA:47612 · Occasional (29-5%)
- GJC2-related late-onset primary lymphedemaORPHA:568051 · Occasional (29-5%)
- Legionnaires diseaseORPHA:549 · Occasional (29-5%)
- MelioidosisORPHA:31202 · Occasional (29-5%)
- Microcephaly-chorioretinopathy-lymphedema syndromeORPHA:2526 · Occasional (29-5%)
- Nasolacrimal duct cystORPHA:141083 · Occasional (29-5%)
- Non-syndromic agammaglobulinemiaORPHA:229717 · Occasional (29-5%)
- RetinoblastomaORPHA:790 · Occasional (29-5%)
- Selective IgM deficiencyORPHA:331235 · Occasional (29-5%)
- Tumor necrosis factor receptor 1 associated periodic syndromeORPHA:32960 · Occasional (29-5%)
- ZygomycosisORPHA:73263 · Occasional (29-5%)
- FusariosisORPHA:228119 · Very rare (<4-1%)
- NocardiosisORPHA:31204 · Very rare (<4-1%)
- WHIM syndromeORPHA:51636 · Very rare (<4-1%)
- X-linked hypophosphatemiaORPHA:89936 · Very rare (<4-1%)