Dermatomyositis

A type of idiopathic inflammatory myopathy characterized by evocative skin lesions and symmetrical proximal muscle weakness.



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Narrow down the case reports



Total: 1310 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
1
(39.8%)
21057726
(5763936)
Palpebral involvement as a presenting and sole manifestation of discoid lupus erythematosus.
Yaghoobi R, Feily A, Behrooz B, Yaghoobi E, Mokhtarzadeh S.
ScientificWorldJournal. 2010;10:2130-1.
Blepharitis Scarring
Adult Blepharitis Differential Diagnosis Females Homo sapiens Lupus Erythematosus, Discoid
1
(39.8%)
17992461
Dermatomyositis: an association of gingival telangiectases and anti Jo-1 antibody in the adult.
Dourmishev LA, Dourmishev AL, Schwartz RA.
Acta Dermatovenerol Alp Pannonica Adriat. 2007;16(2):67-72.
Erythema of the eyelids Myositis
Antibodies, Antinuclear Dermatomyositis Females Gingival Diseases Homo sapiens Middle Aged Skin Telangiectasis
1
(39.8%)
8829501
Low-dose methotrexate as an adjunctive therapy with surgery for ectropion complicating dermatomyositis.
Abernethy ML, Arterberry JF, Callen JP.
Dermatology. 1996;192(2):153-5.
Entropion Scarring
Adult Conjunctivitis Dermatologic Agents Dermatomyositis Dose-Response Relationship, Drug Ectropion Females Homo sapiens
4
(39.3%)
8235910
[Two cases of acute progressive interstitial pneumonia associated with dermatomyositis--clinical features and immunological disorders].
Okuda Y, Takasugi K, Imai A, Oyama T, Oyama H.
Ryumachi. 1993;33(4):293-301.
Arthritis Stomatitis
PIK3C2A
Acute Disease Adult Bronchoalveolar Lavage Fluid Dermatomyositis Fatal Outcome Females Homo sapiens Lymphocyte Subset Middle Aged Pulmonary Fibrosis
5
(38.4%)
8297066
Exuberant conjunctival pseudopolyposis in a patient with dermatomyositis.
Ibanez HE, Bardenstein DS, Korman NJ, Reinhart WJ.
Ann Ophthalmol. 1993;25(9):326-7.
Conjunctivitis Inflammatory myopathy
Conjunctival Diseases Corneal Diseases Dermatomyositis Females Homo sapiens Middle Aged
6
(37.8%)
19995656
[Interstitial pneumonia complicating amyopathic dermatomyositis: a case report].
Jamoussi SK, Dhaou BB, Boussema F, Kochbati S, Baili L, Aouina H, Cherif O, Bouacha H, Rokbani L.
Rev Pneumol Clin. 2009;65(6):353-6.
Arthritis Periorbital edema
Autoantibodies Combination Drug Therapy Dermatomyositis Dyspnea Fatal Outcome Females Homo sapiens Immunosuppressive Agents Lung Diseases, Interstitial Middle Aged X-Ray Computed Tomography
7
(37.2%)
10027999
Periorbital edema as the presenting sign of juvenile dermatomyositis.
Sevigny GM, Mathes BM.
Pediatr Dermatol. 1999;16(1):43-5.
Subcutaneous calcification Periorbital edema
Child, Preschool Dermatomyositis Differential Diagnosis Edema Females Homo sapiens
8
(36.8%)
30365479
Unilateral Eyelid Swelling as a Sign of Antimelanoma Differentiation-Associated Gene 5 (Anti-MDA5)-Antibody-Positive Dermatomyositis.
Lam SC, Yuen HKL.
Ophthalmic Plast Reconstr Surg. 2018;34(6):e209-e211.
Oral ulcer Muscle weakness
IFIH1
Adult Autoantibodies Biopsy Dermatomyositis Differential Diagnosis Edema Eyelid Diseases Females Homo sapiens Interferon-Induced Helicase, IFIH1
8
(36.8%)
29507032
Following leads: connecting dysphagia to mixed connective tissue disease.
Gameiro RS, Reis AIA, Grilo AC, Noronha C.
BMJ Case Rep. 2018;2018:.
Easy fatigability Tongue atrophy
Deglutition Disorders Delayed Diagnosis Disease Progression Females Homo sapiens Middle Aged Mixed Connective Tissue Disease Muscle Weakness
8
(36.8%)
21779715
Paraneoplastic vesiculobullous dermatomyositis with synchronic prostate and tongue tumors: case report.
Caratta PR, Mafort T, Pamplona M, Schau B, Estrella RR, Ramos RC.
Rev Bras Reumatol. 2011;51(4):394-6, 407.
Myopathy Squamous cell carcinoma of the tongue
Dermatomyositis Homo sapiens Male Neoplasms, Multiple Primary Paraneoplastic Syndromes Prostatic Neoplasms Skin Diseases, Vesiculobullous Tongue Neoplasms
        

Phenotype(s) retrieved from Orphanet

    Total: 49

HPO ID Term Frequency
HP:0000492 Abnormal eyelid morphology Very frequent (99-80%)
HP:0000969 Edema Very frequent (99-80%)
HP:0002960 Autoimmunity Very frequent (99-80%)
HP:0003326 Myalgia Very frequent (99-80%)
HP:0003457 EMG abnormality Very frequent (99-80%)
HP:0003701 Proximal muscle weakness Very frequent (99-80%)
HP:0009071 Inflammatory myopathy Very frequent (99-80%)
HP:0010783 Erythema Very frequent (99-80%)
HP:0100539 Periorbital edema Very frequent (99-80%)
HP:0000934 Chondrocalcinosis Frequent (79-30%)
HP:0000958 Dry skin Frequent (79-30%)
HP:0000989 Pruritus Frequent (79-30%)
HP:0001063 Acrocyanosis Frequent (79-30%)
HP:0001252 Muscular hypotonia Frequent (79-30%)
HP:0001369 Arthritis Frequent (79-30%)
HP:0001597 Abnormality of the nail Frequent (79-30%)
HP:0001824 Weight loss Frequent (79-30%)
HP:0002093 Respiratory insufficiency Frequent (79-30%)
HP:0002205 Recurrent respiratory infections Frequent (79-30%)
HP:0002206 Pulmonary fibrosis Frequent (79-30%)
HP:0002207 Diffuse reticular or finely nodular infiltrations Frequent (79-30%)
HP:0002829 Arthralgia Frequent (79-30%)
HP:0006530 Interstitial pulmonary abnormality Frequent (79-30%)
HP:0011362 Abnormal hair quantity Frequent (79-30%)
HP:0012378 Fatigue Frequent (79-30%)
HP:0200034 Papule Frequent (79-30%)
HP:0200042 Skin ulcer Frequent (79-30%)
HP:0000992 Cutaneous photosensitivity Occasional (29-5%)
HP:0001608 Abnormality of the voice Occasional (29-5%)
HP:0001618 Dysphonia Occasional (29-5%)
HP:0001658 Myocardial infarction Occasional (29-5%)
HP:0001701 Pericarditis Occasional (29-5%)
HP:0001879 Abnormal eosinophil morphology Occasional (29-5%)
HP:0001945 Fever Occasional (29-5%)
HP:0002092 Pulmonary arterial hypertension Occasional (29-5%)
HP:0002633 Vasculitis Occasional (29-5%)
HP:0002664 Neoplasm Occasional (29-5%)
HP:0002665 Lymphoma Occasional (29-5%)
HP:0003002 Breast carcinoma Occasional (29-5%)
HP:0008065 Aplasia/Hypoplasia of the skin Occasional (29-5%)
HP:0008872 Feeding difficulties in infancy Occasional (29-5%)
HP:0011675 Arrhythmia Occasional (29-5%)
HP:0011703 Sinus tachycardia Occasional (29-5%)
HP:0012819 Myocarditis Occasional (29-5%)
HP:0030078 Lung adenocarcinoma Occasional (29-5%)
HP:0100585 Telangiectasia of the skin Occasional (29-5%)
HP:0100658 Cellulitis Occasional (29-5%)
HP:0100723 Gastrointestinal stroma tumor Occasional (29-5%)
HP:0100758 Gangrene Occasional (29-5%)


Phenotype(s) retrieved from case reports

    Total: 252

HPO ID Term # of case reports
HP:0100614 Myositis 67
HP:0002090 Pneumonia 66
HP:0001370 Rheumatoid arthritis 57
HP:0009071 Inflammatory myopathy 46
HP:0001324 Muscle weakness 39
HP:0025421 Pneumomediastinum 39
HP:0030731 Carcinoma 38
HP:0002861 Melanoma 35
HP:0003761 Calcinosis 35
HP:0003198 Myopathy 34
HP:0010783 Erythema 29
HP:0012490 Panniculitis 29
HP:0003701 Proximal muscle weakness 27
HP:0000988 Skin rash 22
HP:0025508 Gottron's papules 19
HP:0002664 Neoplasm 18
HP:0012115 Hepatitis 18
HP:0040324 Heliotrope rash 16
HP:0000969 Edema 15
HP:0002097 Emphysema 14
HP:0001945 Fever 13
HP:0002015 Dysphagia 13
HP:0002206 Pulmonary fibrosis 13
HP:0025520 Calcinosis cutis 12
HP:0006515 Interstitial pneumonitis 11
HP:0001369 Arthritis 10
HP:0002878 Respiratory failure 10
HP:0000819 Diabetes mellitus 8
HP:0000956 Acanthosis nigricans 8
HP:0001009 Telangiectasia 8
HP:0001019 Erythroderma 8
HP:0030078 Lung adenocarcinoma 8
HP:0200034 Papule 8
HP:0000488 Retinopathy 7
HP:0003003 Colon cancer 7
HP:0005523 Lymphoproliferative disorder 7
HP:0025318 Ovarian carcinoma 7
HP:0000099 Glomerulonephritis 6
HP:0001909 Leukemia 6
HP:0002107 Pneumothorax 6
HP:0002716 Lymphadenopathy 6
HP:0003201 Rhabdomyolysis 6
HP:0025535 Shawl sign 6
HP:0100539 Periorbital edema 6
HP:0100646 Thyroiditis 6
HP:0000822 Hypertension 5
HP:0000989 Pruritus 5
HP:0001025 Urticaria 5
HP:0002860 Squamous cell carcinoma 5
HP:0003326 Myalgia 5
HP:0006740 Transitional cell carcinoma of the bladder 5
HP:0008978 Necrotizing myopathy 5
HP:0032252 Granuloma 5
HP:0100537 Fasciitis 5
HP:0200042 Skin ulcer 5
HP:0000790 Hematuria 4
HP:0000939 Osteoporosis 4
HP:0001029 Poikiloderma 4
HP:0001482 Subcutaneous nodule 4
HP:0001658 Myocardial infarction 4
HP:0001824 Weight loss 4
HP:0002027 Abdominal pain 4
HP:0002094 Dyspnea 4
HP:0002202 Pleural effusion 4
HP:0002955 Granulomatosis 4
HP:0012819 Myocarditis 4
HP:0025615 Abscess 4
HP:0200123 Chronic hepatitis 4
HP:0000100 Nephrotic syndrome 3
HP:0000112 Nephropathy 3
HP:0000821 Hypothyroidism 3
HP:0000979 Purpura 3
HP:0001638 Cardiomyopathy 3
HP:0001873 Thrombocytopenia 3
HP:0002093 Respiratory insufficiency 3
HP:0002102 Pleuritis 3
HP:0002204 Pulmonary embolism 3
HP:0002913 Myoglobinuria 3
HP:0007430 Generalized edema 3
HP:0007618 Subcutaneous calcification 3
HP:0011838 Sclerodactyly 3
HP:0012050 Anasarca 3
HP:0012125 Prostate cancer 3
HP:0012344 Morphea 3
HP:0012378 Fatigue 3
HP:0030357 Small cell lung carcinoma 3
HP:0100279 Ulcerative colitis 3
HP:0100658 Cellulitis 3
HP:0100806 Sepsis 3
HP:0000093 Proteinuria 2
HP:0000155 Oral ulcer 2
HP:0000572 Visual loss 2
HP:0000709 Psychosis 2
HP:0000855 Insulin resistance 2
HP:0001036 Parakeratosis 2
HP:0001051 Seborrheic dermatitis 2
HP:0001250 Seizures 2
HP:0001394 Cirrhosis 2
HP:0001635 Congestive heart failure 2
HP:0001701 Pericarditis 2
HP:0001876 Pancytopenia 2
HP:0001880 Eosinophilia 2
HP:0002024 Malabsorption 2
HP:0002098 Respiratory distress 2
HP:0002588 Duodenal ulcer 2
HP:0002721 Immunodeficiency 2
HP:0002960 Autoimmunity 2
HP:0003040 Arthropathy 2
HP:0003072 Hypercalcemia 2
HP:0003470 Paralysis 2
HP:0009073 Progressive proximal muscle weakness 2
HP:0011974 Myelofibrosis 2
HP:0012126 Stomach cancer 2
HP:0012151 Hemothorax 2
HP:0012722 Heart block 2
HP:0012735 Cough 2
HP:0030394 Fallopian tube carcinoma 2
HP:0031273 Shock 2
HP:0031690 Opportunistic infection 2
HP:0032379 Polymorphous light eruption 2
HP:0100519 Anuria 2
HP:0100584 Endocarditis 2
HP:0100601 Eclampsia 2
HP:0100726 Kaposi's sarcoma 2
HP:0200120 Chronic active hepatitis 2
HP:0000071 Ureteral stenosis 1
HP:0000083 Renal insufficiency 1
HP:0000123 Nephritis 1
HP:0000282 Facial edema 1
HP:0000544 External ophthalmoplegia 1
HP:0000602 Ophthalmoplegia 1
HP:0000621 Entropion 1
HP:0000656 Ectropion 1
HP:0000726 Dementia 1
HP:0000763 Sensory neuropathy 1
HP:0000824 Growth hormone deficiency 1
HP:0000843 Hyperparathyroidism 1
HP:0000964 Eczema 1
HP:0001041 Facial erythema 1
HP:0001047 Atopic dermatitis 1
HP:0001217 Clubbing 1
HP:0001269 Hemiparesis 1
HP:0001271 Polyneuropathy 1
HP:0001279 Syncope 1
HP:0001287 Meningitis 1
HP:0001289 Confusion 1
HP:0001297 Stroke 1
HP:0001513 Obesity 1
HP:0001541 Ascites 1
HP:0001618 Dysphonia 1
HP:0001649 Tachycardia 1
HP:0001698 Pericardial effusion 1
HP:0001733 Pancreatitis 1
HP:0001735 Acute pancreatitis 1
HP:0001878 Hemolytic anemia 1
HP:0001891 Iron deficiency anemia 1
HP:0001903 Anemia 1
HP:0001919 Acute kidney injury 1
HP:0002014 Diarrhea 1
HP:0002017 Nausea and vomiting 1
HP:0002035 Rectal prolapse 1
HP:0002039 Anorexia 1
HP:0002072 Chorea 1
HP:0002099 Asthma 1
HP:0002108 Spontaneous pneumothorax 1
HP:0002113 Pulmonary infiltrates 1
HP:0002140 Ischemic stroke 1
HP:0002155 Hypertriglyceridemia 1
HP:0002176 Spinal cord compression 1
HP:0002240 Hepatomegaly 1
HP:0002315 Headache 1
HP:0002352 Leukoencephalopathy 1
HP:0002411 Myokymia 1
HP:0002563 Constrictive pericarditis 1
HP:0002592 Gastric ulcer 1
HP:0002615 Hypotension 1
HP:0002617 Dilatation 1
HP:0002719 Recurrent infections 1
HP:0002762 Multiple exostoses 1
HP:0002829 Arthralgia 1
HP:0002835 Aspiration 1
HP:0002862 Bladder carcinoma 1
HP:0002863 Myelodysplasia 1
HP:0002905 Hyperphosphatemia 1
HP:0002907 Microscopic hematuria 1
HP:0003095 Septic arthritis 1
HP:0003236 Elevated serum creatine kinase 1
HP:0003690 Limb muscle weakness 1
HP:0004326 Cachexia 1
HP:0004756 Ventricular tachycardia 1
HP:0004942 Aortic aneurysm 1
HP:0005110 Atrial fibrillation 1
HP:0005145 Coronary artery stenosis 1
HP:0005162 Left ventricular dysfunction 1
HP:0005263 Gastritis 1
HP:0005268 Spontaneous abortion 1
HP:0006946 Recurrent meningitis 1
HP:0007178 Motor polyneuropathy 1
HP:0007502 Follicular hyperkeratosis 1
HP:0008682 Acute tubular necrosis 1
HP:0009125 Lipodystrophy 1
HP:0009792 Teratoma 1
HP:0009830 Peripheral neuropathy 1
HP:0009831 Mononeuropathy 1
HP:0010310 Chylothorax 1
HP:0010766 Ectopic calcification 1
HP:0011531 Vitritis 1
HP:0011675 Arrhythmia 1
HP:0011704 Sick sinus syndrome 1
HP:0011951 Aspiration pneumonia 1
HP:0012085 Pyuria 1
HP:0012089 Arteritis 1
HP:0012114 Endometrial carcinoma 1
HP:0012156 Hemophagocytosis 1
HP:0012188 Hyperemesis gravidarum 1
HP:0012226 Ovarian teratoma 1
HP:0012234 Agranulocytosis 1
HP:0012251 ST segment elevation 1
HP:0012315 Histiocytoma 1
HP:0012432 Chronic fatigue 1
HP:0012486 Myelitis 1
HP:0012531 Pain 1
HP:0012578 Membranous nephropathy 1
HP:0012636 Retinal vein occlusion 1
HP:0012733 Macule 1
HP:0025142 Constitutional symptom 1
HP:0025342 Central retinal artery occlusion 1
HP:0025388 Thyroid nodule 1
HP:0025406 Asthenia 1
HP:0025637 Vasospasm 1
HP:0030157 Flank pain 1
HP:0030413 Squamous cell carcinoma of the tongue 1
HP:0030449 Therapeutic abortion 1
HP:0030808 Ragged cuticle 1
HP:0030833 Neck pain 1
HP:0030880 Raynaud phenomenon 1
HP:0031274 Hypovolemic shock 1
HP:0031368 Intestinal perforation 1
HP:0032118 Retinitis 1
HP:0032245 Abnormal metabolism 1
HP:0032282 Contact dermatitis 1
HP:0100295 Muscle fiber atrophy 1
HP:0100550 Tendon rupture 1
HP:0100578 Lipoatrophy 1
HP:0100633 Esophagitis 1
HP:0100644 Melanonychia 1
HP:0100665 Angioedema 1
HP:0100749 Chest pain 1
HP:0100769 Synovitis 1
HP:0100825 Cheilitis 1
HP:0200039 Pustule 1
HP:0200119 Acute hepatitis 1


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID