Proliferating Trichilemmal Cyst |
|
Skin ulcer, Epidermoid cyst |
ORPHA:492 |
Non-Epidermolytic Palmoplantar Keratoderma |
|
Erythema, Skin ulcer, Papule |
ORPHA:2337 |
Immunodeficiency 107, Susceptibility To Invasive Staphylococcus Aureus Infection |
|
Pyoderma gangrenosum |
OMIM:619986 |
Dermatofibrosarcoma Protuberans |
|
Skin ulcer, Subcutaneous nodule, Erythema |
ORPHA:31112 |
Hyperkeratosis Lenticularis Perstans |
|
Skin ulcer, Aplasia/Hypoplasia of the skin, Papule |
ORPHA:409 |
Congenital Factor Xii Deficiency |
|
Penetrating foot ulcers |
ORPHA:330 |
Necrobiosis Lipoidica |
|
Annular cutaneous lesion, Atrophic scars, Skin ulcer, Skin nodule, Papule, Skin plaque, Erythema,... |
ORPHA:542592 |
Chilblain Lupus 1 |
|
Skin ulcer |
OMIM:610448 |
Juvenile Hyaline Fibromatosis |
|
Skin ulcer, Subcutaneous nodule, Aplasia/Hypoplasia of the skin, Papule |
ORPHA:2028 |
Aplasia Cutis Congenita |
|
Congenital localized absence of skin, Aplasia cutis congenita over the scalp vertex, Skin ulcer |
ORPHA:1114 |
Aplasia Cutis-Myopia Syndrome |
|
Skin ulcer, Aplasia cutis congenita |
ORPHA:1117 |
Severe Hereditary Thrombophilia Due To Congenital Protein S Deficiency |
|
Thin skin, Skin ulcer, Purpura, Aplasia/Hypoplasia of the skin |
ORPHA:743 |
Buerger Disease |
|
Skin ulcer |
ORPHA:36258 |
Dracunculiasis |
|
Skin ulcer, Subcutaneous nodule |
ORPHA:231 |
Acrogeria |
|
Thin skin, Skin ulcer, Aplasia/Hypoplasia of the skin, Excessive wrinkled skin |
ORPHA:2500 |
Familial Keratoacanthoma |
|
Skin ulcer, Subcutaneous nodule, Papule |
ORPHA:493 |
Classic Mycosis Fungoides |
|
Skin ulcer, Hypopigmented skin patches, Skin plaque, Erythema, Dry skin |
ORPHA:2584 |
Mutilating Hereditary Sensory Neuropathy With Spastic Paraplegia |
|
Acral ulceration, Skin ulcer |
ORPHA:139578 |
Cervical Hypertrichosis-Peripheral Neuropathy Syndrome |
|
Skin ulcer |
ORPHA:2218 |
Lichen Planopilaris |
|
Dermal atrophy, Skin ulcer, Papule, Hypopigmented skin patches |
ORPHA:525 |
Chilblain Lupus |
|
Erythematous papule, Skin ulcer |
ORPHA:90280 |
Brooke-Spiegler Syndrome |
|
Nodular changes affecting the eyelids, Skin-colored papule, Skin ulcer, Skin nodule |
ORPHA:79493 |
Limited Cutaneous Systemic Sclerosis |
|
Skin ulcer, Hypopigmented skin patches |
ORPHA:220402 |
Subcutaneous Panniculitis-Like T-Cell Lymphoma |
|
Erythematous plaque, Erythematous papule, Skin ulcer |
ORPHA:86884 |
Pyoderma Gangrenosum |
|
Skin vesicle, Atrophic scars, Skin ulcer, Papule |
ORPHA:48104 |
Ollier Disease |
|
Skin ulcer, Subcutaneous nodule |
ORPHA:296 |
Familial Multiple Nevi Flammei |
|
Hypermelanotic macule, Skin ulcer, Papule, Nevus flammeus |
ORPHA:624 |
Bare Lymphocyte Syndrome, Type I |
|
Skin ulcer |
OMIM:604571 |
Autosomal Dominant Epidermolytic Ichthyosis |
|
Skin ulcer |
ORPHA:312 |
Leishmaniasis |
|
Skin plaque, Skin ulcer, Papule, Pallor |
ORPHA:507 |
Hemoglobin D Disease |
|
Anemia, Reduced alpha/beta synthesis ratio, HbS hemoglobin, Increased HbA2 hemoglobin, Reduced he... |
ORPHA:90039 |
Polyarteritis Nodosa |
|
Skin ulcer, Subcutaneous nodule, Erythema |
ORPHA:767 |
Reticular Dysgenesis |
|
Skin ulcer |
ORPHA:33355 |
Flynn-Aird Syndrome |
|
Dermal atrophy, Skin ulcer |
ORPHA:2047 |
Combined Immunodeficiency Due To Dock8 Deficiency |
|
Skin ulcer |
ORPHA:217390 |
Adult Polyglucosan Body Disease |
|
Skin ulcer |
ORPHA:206583 |
Attenuated Chédiak-Higashi Syndrome |
|
Skin ulcer |
ORPHA:352723 |
Hereditary Sensory And Autonomic Neuropathy Type 1 |
|
Penetrating foot ulcers, Skin ulcer |
ORPHA:36386 |
Beta-Thalassemia |
|
Skin ulcer, Pallor |
ORPHA:848 |
Acquired Purpura Fulminans |
|
Macular purpura, Macule, Pyoderma gangrenosum, Erythematous macule |
ORPHA:49566 |
Neuropathy, Hereditary Sensory And Autonomic, Type Ic |
|
Skin ulcer |
OMIM:613640 |
Calciphylaxis |
|
Skin ulcer |
ORPHA:280062 |
Dermatoosteolysis, Kirghizian Type |
|
Skin ulcer, Aplasia/Hypoplasia of the skin |
ORPHA:1657 |
Isolated Agammaglobulinemia |
|
Skin ulcer |
ORPHA:229717 |
Squamous Cell Carcinoma Of The Anal Canal |
|
Skin ulcer |
ORPHA:424019 |
Pyogenic Arthritis-Pyoderma Gangrenosum-Acne Syndrome |
|
Skin ulcer |
ORPHA:69126 |
Free Sialic Acid Storage Disease |
|
Skin ulcer |
ORPHA:834 |
Pyogenic Sterile Arthritis, Pyoderma Gangrenosum, And Acne |
|
Pyoderma gangrenosum |
OMIM:604416 |
Prolidase Deficiency |
|
Thin skin, Skin ulcer, Papule, Aplasia/Hypoplasia of the skin, Erythema, Dry skin |
ORPHA:742 |
Takayasu Arteritis |
|
Skin ulcer, Subcutaneous nodule |
ORPHA:3287 |
Immunodeficiency, Common Variable, 12, With Autoimmunity |
|
Pyoderma gangrenosum |
OMIM:616576 |
Infantile Myofibromatosis |
|
Skin ulcer, Subcutaneous nodule |
ORPHA:2591 |
Meige Disease |
|
Skin dimple, Atypical scarring of skin, Skin ulcer, Skin erosion |
ORPHA:90186 |
Mutilating Palmoplantar Keratoderma With Periorificial Keratotic Plaques |
|
Skin fissure, Skin ulcer, Erythema |
ORPHA:659 |
Cryoglobulinemic Vasculitis |
|
Skin ulcer, Purpura, Petechiae |
ORPHA:91138 |
Periodic Fever, Immunodeficiency, And Thrombocytopenia Syndrome |
|
Pyoderma gangrenosum |
OMIM:150550 |
Neutrophilic Dermatosis, Acute Febrile |
|
Pyoderma gangrenosum, Erythema |
OMIM:608068 |
X-Linked Agammaglobulinemia |
|
Skin ulcer, Hypopigmented skin patches |
ORPHA:47 |
Epidermolysis Bullosa, Junctional 2C, Laryngoonychocutaneous |
|
Skin ulcer |
OMIM:245660 |
Chronic Granulomatous Disease |
|
Macule, Skin ulcer, Hypermelanotic macule |
ORPHA:379 |
Prolidase Deficiency |
|
Skin ulcer, Petechiae |
OMIM:170100 |
Autosomal Dominant Hyper-Ige Syndrome |
|
Skin vesicle, Skin ulcer, Papule |
ORPHA:2314 |
Adult Syndrome |
|
Thin skin, Skin ulcer, Melanocytic nevus, Dry skin |
ORPHA:978 |
Diamond-Blackfan Anemia 16 |
|
Anemia, Pulmonic stenosis, Atrial septal defect |
OMIM:617408 |
Chronic Mucocutaneous Candidiasis |
|
Papule, Skin ulcer, Erythema |
ORPHA:1334 |
Attrv122I Amyloidosis |
|
Anemia, Restrictive cardiomyopathy, Reduced left ventricular ejection fraction, Abnormal EKG, Lef... |
ORPHA:85451 |
Reynolds Syndrome |
|
Skin ulcer |
ORPHA:779 |
Livedoid Vasculopathy |
|
Macular purpura, Atrophic scars, Skin ulcer, Ecchymosis, Erythematous papule |
ORPHA:542643 |
Ectodermal Dysplasia-Blindness Syndrome |
|
Skin ulcer |
ORPHA:1806 |
Microscopic Polyangiitis |
|
Skin ulcer, Subcutaneous nodule, Erythema |
ORPHA:727 |
Peripartum Cardiomyopathy |
|
Sinus tachycardia, Cardiogenic shock, Palpitations, Elevated jugular venous pressure, Abnormal at... |
ORPHA:563 |
Werner Syndrome |
|
Lack of skin elasticity, Skin ulcer, Aplasia/Hypoplasia of the skin |
ORPHA:902 |
Acrodermatitis Enteropathica |
|
Skin ulcer, Dry skin, Erythema |
ORPHA:37 |
Infantile Systemic Hyalinosis |
|
Skin ulcer, Subcutaneous nodule |
ORPHA:2176 |
Diffuse Cutaneous Systemic Sclerosis |
|
Skin ulcer |
ORPHA:220393 |
Hereditary Spherocytosis |
|
Skin ulcer, Pallor |
ORPHA:822 |
Beta-Thalassemia Intermedia |
|
Skin ulcer, Pallor |
ORPHA:231222 |
Autosomal Dominant Severe Congenital Neutropenia |
|
Pyoderma gangrenosum |
ORPHA:486 |
Hemolytic Anemia Due To Red Cell Pyruvate Kinase Deficiency |
|
Anemia, Congenital hemolytic anemia, Reticulocytosis, Poikilocytosis, Abnormal erythrocyte morpho... |
ORPHA:766 |
Sweet Syndrome |
|
Skin vesicle, Pyoderma gangrenosum, Skin nodule, Erythematous plaque, Erythematous papule |
ORPHA:3243 |
Malakoplakia |
|
Skin ulcer, Subcutaneous nodule, Papule |
ORPHA:556 |
Fusariosis |
|
Skin detachment, Skin ulcer, Subcutaneous nodule, Papule |
ORPHA:228119 |
Hereditary Acrokeratotic Poikiloderma |
|
Thin skin, Skin ulcer, Papule, Hypopigmented skin patches, Erythema |
ORPHA:2907 |
Catastrophic Antiphospholipid Syndrome |
|
Skin ulcer |
ORPHA:464343 |
Neonatal Lupus Erythematosus |
|
Anemia, Neutropenia, Hemolytic anemia, Hydrocephalus, Dilated cardiomyopathy, Pancytopenia, Heart... |
ORPHA:398124 |
Anemia, Congenital Dyserythropoietic, Type Iv |
|
Anemia, Reduced hematocrit, Hemolytic anemia, Circulating nucleated red blood cells, Erythroid hy... |
OMIM:613673 |
Immunoglobulin A Vasculitis |
|
Macule, Skin ulcer, Purpura, Erythema |
ORPHA:761 |
Juvenile Dermatomyositis |
|
Skin ulcer, Dry skin, Erythema |
ORPHA:93672 |
Dyskeratosis Congenita |
|
Skin vesicle, Skin ulcer, Hypopigmented skin patches, Macule, Aplasia/Hypoplasia of the skin, Hyp... |
ORPHA:1775 |
Leukocyte Adhesion Deficiency, Type I |
|
Skin ulcer |
OMIM:116920 |
Giant Cell Arteritis |
|
Skin ulcer |
ORPHA:397 |
Dominant Beta-Thalassemia |
|
Skin ulcer, Pallor |
ORPHA:231226 |
Hb Bart'S Hydrops Fetalis |
|
Anemia, Hydrocephalus, Congestive heart failure, Pericarditis, Abnormal hemoglobin, Splenomegaly |
ORPHA:163596 |
Toxic Epidermal Necrolysis |
|
Macule, Skin ulcer, Erythema |
ORPHA:537 |
Parkes Weber Syndrome |
|
Erythematous plaque, Scaling skin, Skin ulcer, Capillary malformation |
ORPHA:90307 |
Beta-Thalassemia Major |
|
Skin ulcer, Pallor |
ORPHA:231214 |
Incontinentia Pigmenti |
|
Skin ulcer, Erythema, Hypopigmented skin patches |
ORPHA:464 |
Adenocarcinoma Of The Anal Canal |
|
Skin ulcer |
ORPHA:424016 |
Blau Syndrome |
|
Skin ulcer, Intermittent generalized erythematous papular rash |
OMIM:186580 |
Granulomatosis With Polyangiitis |
|
Skin ulcer |
OMIM:608710 |
Systemic Sclerosis |
|
Digital pitting scar, Spotty hypopigmentation, Digital ulcer, Acral ulceration, Cutaneous sclerot... |
ORPHA:90291 |
Pgm3-Cdg |
|
Skin ulcer |
ORPHA:443811 |
Dermatomyositis |
|
Skin ulcer, Papule, Aplasia/Hypoplasia of the skin, Erythema, Dry skin |
ORPHA:221 |
Vasculitis, Autoinflammation, Immunodeficiency, And Hematologic Defects Syndrome |
|
Urticarial plaque, Skin ulcer, Purpura |
OMIM:615688 |
Amoebiasis Due To Free-Living Amoebae |
|
Skin ulcer, Subcutaneous nodule, Papule |
ORPHA:68 |
Microcephaly-Lymphedema-Chorioretinopathy Syndrome |
|
Scaling skin, Skin ulcer, Subcutaneous nodule, Dry skin |
ORPHA:2526 |
Angioosteohypertrophic Syndrome |
|
Hyperpigmented nevi, Skin ulcer, Melanocytic nevus |
ORPHA:2346 |
Charcot-Marie-Tooth Disease Type 4B2 |
|
Penetrating foot ulcers |
ORPHA:99956 |
Leprosy |
|
Urticarial plaque, Skin nodule, Acral ulceration, Hypopigmented macule, Verrucous papule, Penetra... |
ORPHA:548 |
Chime Syndrome |
|
Skin ulcer, Erythema |
ORPHA:3474 |
Diamond-Blackfan Anemia 10 |
|
Patent ductus arteriosus, Anemia, Ventricular septal defect, Steroid-responsive anemia, Reticuloc... |
OMIM:613309 |
Wiskott-Aldrich Syndrome |
|
Skin ulcer, Purpura, Petechiae |
ORPHA:906 |
Hajdu-Cheney Syndrome |
|
Skin ulcer, Dry skin |
ORPHA:955 |
Cushing Disease |
|
Thin skin, Striae distensae, Skin ulcer, Purpura, Ecchymosis |
ORPHA:96253 |
Granulomatosis With Polyangiitis |
|
Skin ulcer, Purpura, Papule |
ORPHA:900 |
Primary Sjögren Syndrome |
|
Dry skin, Skin ulcer, Purpura, Lichenoid skin lesion |
ORPHA:289390 |
Oculocerebrorenal Syndrome Of Lowe |
|
Atypical scarring of skin, Skin ulcer |
ORPHA:534 |
Blau Syndrome |
|
Papule, Skin ulcer, Dry skin, Erythema |
ORPHA:90340 |
Atypical Werner Syndrome |
|
Lack of skin elasticity, Thin skin, Skin ulcer, Aplasia/Hypoplasia of the skin |
ORPHA:79474 |
Gaucher Disease-Ophthalmoplegia-Cardiovascular Calcification Syndrome |
|
Skin ulcer, Ecchymosis |
ORPHA:2072 |
Chronic Graft Versus Host Disease |
|
Skin vesicle, Skin ulcer, Intermittent generalized erythematous papular rash, Erythema |
ORPHA:99921 |
Plague |
|
Localized skin lesion, Skin ulcer, Dry skin |
ORPHA:707 |
Cushing Syndrome Due To Ectopic Acth Secretion |
|
Thin skin, Striae distensae, Skin ulcer, Purpura, Ecchymosis |
ORPHA:99889 |
Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis Spectrum |
|
Atypical scarring of skin, Skin ulcer |
ORPHA:95455 |
Split Cord Malformation |
|
Skin dimple, Penetrating foot ulcers |
ORPHA:573278 |
Telangiectasia, Hereditary Hemorrhagic, Type 2 |
|
Facial telangiectasia, Ischemic stroke, Spontaneous, recurrent epistaxis, Fingerpad telangiectase... |
OMIM:600376 |
Leukocyte Adhesion Deficiency |
|
Pyoderma gangrenosum |
ORPHA:2968 |
Homozygous Familial Hypercholesterolemia |
|
Aortic atherosclerotic lesion, Abnormal tendon morphology, Tendon xanthomatosis, Premature arteri... |
ORPHA:391665 |
Visceral Steatosis, Congenital |
|
Neonatal death, Myocardial steatosis |
OMIM:228100 |
Fibronectin Glomerulopathy |
|
Hypoalbuminemia |
ORPHA:84090 |
Spondylometaphyseal Dysplasia, 'Corner Fracture' Type |
|
Iron deficiency anemia |
ORPHA:93315 |
Glomerulopathy With Fibronectin Deposits 2 |
|
Hypertension |
OMIM:601894 |
Spondylometaphyseal Dysplasia, Corner Fracture Type |
|
Short stature |
OMIM:184255 |