12q14 microdeletion syndrome
|
(Orphanet:94063)
|
Acrokeratoelastoidosis of Costa
|
(Orphanet:38)
|
Adiposis dolorosa
|
(Orphanet:36397)
|
Aggressive systemic mastocytosis
|
(Orphanet:98850)
|
Albright hereditary osteodystrophy
|
(Orphanet:665)
|
Alport syndrome
|
(Orphanet:63)
|
Amelogenesis imperfecta and gingival hyperplasia syndrome
|
(Orphanet:171836)
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Autosomal recessive palmoplantar keratoderma and congenital alopecia
|
(Orphanet:1366)
|
Bazex-Dupré-Christol syndrome
|
(Orphanet:113)
|
Behçet disease
|
(Orphanet:117)
|
Benign cephalic histiocytosis
|
(Orphanet:157997)
|
Blue rubber bleb nevus
|
(Orphanet:1059)
|
COWDEN SYNDROME 5
|
(OMIM:615108)
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COWDEN SYNDROME 6
|
(OMIM:615109)
|
Chylous ascites
|
(Orphanet:1160)
|
Cowden syndrome
|
(Orphanet:201)
|
Cutaneous leukocytoclastic angiitis
|
(Orphanet:889)
|
Cutaneous lupus erythematosus
|
(Orphanet:535)
|
Cutaneous mastocytoma
|
(Orphanet:79455)
|
Cutaneous mastocytosis
|
(Orphanet:66646)
|
Cutis gyrata - acanthosis nigricans - craniosynostosis
|
(Orphanet:1555)
|
Dermatofibrosarcoma protuberans
|
(Orphanet:31112)
|
Desmoid tumor
|
(Orphanet:873)
|
Dissecting cellulitis of the scalp
|
(Orphanet:345)
|
Dracunculiasis
|
(Orphanet:231)
|
Ehlers-Danlos syndrome, hypermobility type
|
(Orphanet:285)
|
Ehlers-Danlos syndrome, vascular type
|
(Orphanet:286)
|
Encephalocraniocutaneous lipomatosis
|
(Orphanet:2396)
|
Enchondromatosis
|
(Orphanet:296)
|
Eosinophilic fasciitis
|
(Orphanet:3165)
|
Eosinophilic granulomatosis with polyangiitis
|
(Orphanet:183)
|
Erythema elevatum diutinum
|
(Orphanet:90000)
|
Fabry disease
|
(Orphanet:324)
|
Familial Dupuytren contracture
|
(Orphanet:79142)
|
Familial cutaneous collagenoma
|
(Orphanet:53296)
|
Familial cylindromatosis
|
(Orphanet:211)
|
Familial keratoacanthoma
|
(Orphanet:493)
|
Familial multiple trichoepithelioma
|
(Orphanet:867)
|
Farber lipogranulomatosis
|
(Orphanet:333)
|
Felty syndrome
|
(Orphanet:47612)
|
Fibrodysplasia ossificans progressiva
|
(Orphanet:337)
|
Focal dermal hypoplasia
|
(Orphanet:2092)
|
Fountain syndrome
|
(Orphanet:3219)
|
Fronto-facio-nasal dysostosis
|
(Orphanet:1791)
|
Gorlin syndrome
|
(Orphanet:377)
|
Hairy cell leukemia variant
|
(Orphanet:300878)
|
Hashimoto-Pritzker syndrome
|
(Orphanet:99872)
|
Hennekam-Beemer syndrome
|
(Orphanet:2135)
|
Hyaluronidase deficiency
|
(Orphanet:67041)
|
Infantile myofibromatosis
|
(Orphanet:2591)
|
Isolated osteopoikilosis
|
(Orphanet:166119)
|
Juvenile Paget disease
|
(Orphanet:2801)
|
Juvenile dermatomyositis
|
(Orphanet:93672)
|
Juvenile hyaline fibromatosis
|
(Orphanet:2028)
|
Juvenile xanthogranuloma
|
(Orphanet:158000)
|
Knuckle pads-leuconychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome
|
(Orphanet:2698)
|
Large congenital melanocytic nevus
|
(Orphanet:626)
|
Lassa fever
|
(Orphanet:99824)
|
Ledderhose disease
|
(Orphanet:199251)
|
Leri pleonosteosis
|
(Orphanet:2900)
|
Lhermitte-Duclos disease
|
(Orphanet:65285)
|
Lipedema
|
(Orphanet:77243)
|
Lipoid proteinosis
|
(Orphanet:530)
|
Liposarcoma
|
(Orphanet:69078)
|
Lyme disease
|
(Orphanet:91546)
|
Maculopapular cutaneous mastocytosis
|
(Orphanet:79457)
|
Maffucci syndrome
|
(Orphanet:163634)
|
Malakoplakia
|
(Orphanet:556)
|
Median nodule of the upper lip
|
(Orphanet:2699)
|
Melorheostosis with osteopoikilosis
|
(Orphanet:1879)
|
Microcephaly - lymphedema - chorioretinopathy
|
(Orphanet:2526)
|
Microscopic polyangiitis
|
(Orphanet:727)
|
Multiple endocrine neoplasia type 1
|
(Orphanet:652)
|
Myxoid/round cell liposarcoma
|
(Orphanet:99967)
|
Nakajo-Nishimura syndrome
|
(Orphanet:2615)
|
Nasopalpebral lipoma - coloboma - telecanthus
|
(Orphanet:2399)
|
Neurofibromatosis type 1
|
(Orphanet:636)
|
Neurofibromatosis type 2
|
(Orphanet:637)
|
Nodular non-suppurative panniculitis
|
(Orphanet:33577)
|
Noonan syndrome with multiple lentigines
|
(Orphanet:500)
|
PTEN hamartoma tumor syndrome
|
(Orphanet:306498)
|
Pai syndrome
|
(Orphanet:1993)
|
Papular xanthoma
|
(Orphanet:158008)
|
Pleomorphic liposarcoma
|
(Orphanet:99969)
|
Porokeratosis
|
(Orphanet:79358)
|
Primary cutaneous anaplastic large cell lymphoma
|
(Orphanet:300865)
|
Primary cutaneous lymphoma
|
(Orphanet:542)
|
Progressive nodular histiocytosis
|
(Orphanet:158022)
|
Progressive osseous heteroplasia
|
(Orphanet:2762)
|
Proteus syndrome
|
(Orphanet:744)
|
Proteus-like syndrome
|
(Orphanet:2969)
|
Pseudoxanthoma elasticum
|
(Orphanet:758)
|
Pyoderma gangrenosum
|
(Orphanet:48104)
|
Pyomyositis
|
(Orphanet:764)
|
Relapsing polychondritis
|
(Orphanet:728)
|
Retinal ischemic syndrome - digestive tract small vessel hyalinosis - diffuse cerebral calcifications
|
(Orphanet:3018)
|
Rhabdoid tumor
|
(Orphanet:69077)
|
Rheumatic fever
|
(Orphanet:3099)
|
Roch-Leri mesosomatous lipomatosis
|
(Orphanet:529)
|
Scleroderma
|
(Orphanet:801)
|
Sea-blue histiocytosis
|
(Orphanet:158029)
|
Segmental outgrowth - lipomatosis - arteriovenous malformation - epidermal nevus
|
(Orphanet:137608)
|
Stiff skin syndrome
|
(Orphanet:2833)
|
Sweet syndrome
|
(Orphanet:3243)
|
Syringocystadenoma papilliferum
|
(Orphanet:840)
|
Takayasu arteritis
|
(Orphanet:3287)
|
Torg-Winchester syndrome
|
(Orphanet:3460)
|
Townes-Brocks syndrome
|
(Orphanet:857)
|
Tuberous sclerosis
|
(Orphanet:805)
|
Tumoral calcinosis
|
(Orphanet:53715)
|
Well-differentiated liposarcoma
|
(Orphanet:99971)
|
Wells syndrome
|
(Orphanet:901)
|