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allergic cutaneous vasculitis +
Alpha-2-Deficient Collagen Disease
arterial tortuosity syndrome
ARTERIAL TORTUOSITY-BONE FRAGILITY SYNDROME
Atrophia Maculosa Varioliformis Cutis, Familial
autoimmune disease of skin and connective tissue +
Autoinflammation with Arthritis and Dyskeratosis
autosomal recessive congenital ichthyosis +
Basaloid Follicular Hamartoma Syndrome, Generalized, Autosomal Dominant
Bloch-Sulzberger syndrome +
Bone Fragility with Contractures, Arterial Rupture, and Deafness
Boudhina Yedes Khiari syndrome
bullous congenital ichthyosiform erythroderma
Buschke-Ollendorff syndrome
chronic interstitial cystitis
Congenital Erythroderma with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-IgE
Congenital Fascial Dystrophy
congenital vertical talus
Connective Tissue Neoplasms +
contagious pustular dermatitis
Cutaneous Bullous Amyloidosis
cutaneous lupus erythematosus +
cutis laxa + A skin disease characterized by loose, hanging, wrinkled skin lacking in elasticity. (DO)
Defect in Hyaluronan Metabolism
Duplication of Eyebrows with Stretchable Skin and Syndactyly
dyschromatosis universalis hereditaria +
Ectodermal Dysplasia-Skin Fragility Syndrome
Eczematous Skin Diseases +
Elastosis Perforans Serpiginosa
Elliott Ludman Teebi Syndrome
endometriosis in scar of skin
epidermolytic hyperkeratosis +
erythematosquamous dermatosis
erythrokeratodermia variabilis +
Familial Reactive Perforating Collagenosis
fibrodysplasia ossificans progressiva
geroderma osteodysplasticum
granulomatosis with polyangiitis +
Hereditary Autoinflammatory Diseases +
Hereditary Sclerosing Poikiloderma +
Hernandez Fragoso Syndrome
Histiocytic Dermatoarthritis
hyaline fibromatosis syndrome
Infectious Skin Diseases +
interstitial lung disease +
Juvenile Spring Eruption of Ears
Keratolytic Winter Erythema
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis
Macroepiphyseal Dysplasia, McAlister Coe Type
Median Cleft Lip, Corpus Callosum, Lipoma, and Skin Polyps
Mental Retardation, Joint Hypermobility, and Skin Laxity, with or without Metabolic Abnormalities
Metabolic Skin Diseases +
multicentric reticulohistiocytosis
multiple cutaneous and mucosal venous malformations
Multiple Noduli Cutanei with Urinary Tract Abnormalities
Necrolytic Migratory Erythema
Nephrogenic Fibrosing Dermopathy
noninfectious dermatoses of eyelid +
orofaciodigital syndrome IX
Papulosquamous Skin Diseases +
Parana Hard Skin Syndrome
Pedal Onychogryposis with Keratosis Plantaris and Coarse Hair
Perifolliculitis Capitis Abscedens Et Suffodiens, Familial
Perioral Pigmented Follicular Atrophoderma with Milia and Epidermoid Cysts
photosensitivity disease +
plasminogen deficiency type I
poikiloderma with neutropenia
primary cutaneous amyloidosis +
progressive osseous heteroplasia
Progressive Vitiligo with Mental Retardation and Urethral Duplication
pseudoxanthoma elasticum +
reactive cutaneous fibrous lesion +
Rothmund-Thomson syndrome +
Roy Maroteaux Kremp Syndrome
sebaceous gland disease +
Sjogren-Larsson syndrome +
spinocerebellar ataxia type 34
systemic lupus erythematosus +
verruciform xanthoma of skin
Vohwinkel Syndrome, Variant Form
X-linked reticulate pigmentary disorder
XEROSIS AND GROWTH FAILURE WITH IMMUNE AND PULMONARY DYSFUNCTION SYNDROME
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