Connective tissue structure

Connective tissue

Connective tissue structure (body structure)

Connective tissue, NOS

21793004

http://purl.bioontology.org/ontology/SNOMEDCT/21793004

0

XU9ex

Systemic fibrosclerosing syndrome

Autosomal recessive pseudoxanthoma elasticum

Polyalgia

Cutis laxa, recessive, type I

Systemic lupus erythematosus-related syndrome

Drug-induced lupus erythematosus

Acquired pseudoxanthoma elasticum

Primary antiphospholipid syndrome with organ/system involvement

SLE glomerulonephritis syndrome, WHO class IV

SLE glomerulonephritis syndrome, WHO class II

Eosinophilic spongiosis (prebullous pemphigus)

Epidermolysis bullosa simplex with neuromuscular disease

Giant cell arteritis with polymyalgia rheumatica

Fulminating systemic lupus erythematosus

Injury of connective tissue

Cantu's syndrome

Localized recessive dystrophic epidermolysis bullosa

Fibrosarcoma of connective tissue

Collagen disease

Connective tissue hereditary disorder

Systemic lupus erythematosus with organ/system involvement

Secondary Sjögren's syndrome with organ/system involvement

Progressive recessive dystrophic epidermolysis bullosa

Marfan's syndrome affecting skin

Pseudosarcomatous fibromatosis

Eosinophilic gastroenteropathy with collagen vascular disease

Lupus anticoagulant disorder

Localized congenital cutis laxa

Cutis laxa, recessive, type II

Generalized junctional epidermolysis bullosa

Systemic lupus erythematosus arthritis

Systemic lupus erythematosus-associated antiphospholipid syndrome

Malignant neoplasm of connective tissue

Keratoconjunctivitis sicca, in Sjögren's syndrome

Epidermolysis bullosa simplex, Ogna type

Collagen deficiency syndrome

Pretibial epidermolysis bullosa

Cutis laxa of upper eyelid

Poikilodermatomyositis

Primary antiphospholipid syndrome with multisystem involvement

Recessive dystrophic epidermolysis bullosa

Autosomal dominant epidermolysis bullosa simplex

Epidermolysis bullosa

Pseudoxanthoma elasticum

Pemphigus neonatorum

Lethal autosomal recessive epidermolysis bullosa simplex

Systemic lupus erythematosus of childhood

Disorder of connective tissue

Dyselastosis with cysts and comedones

Pemphigus vulgaris

SLE glomerulonephritis syndrome

Primary Sjögren's syndrome

Generalized epidermolysis bullosa simplex

Generalized dystrophic epidermolysis bullosa

Congenital connective tissue disorder

Multifocal fibrosclerosis

Drug-induced pseudoxanthoma elasticum

Cutis laxa, autosomal dominant

Cutis laxa senilis

Polymyalgia rheumatica

Gronblad-Strandberg syndrome

Lung disease with Sjögren's disease

Systemic lupus erythematosus with multisystem involvement

SLE glomerulonephritis syndrome, WHO class I

Necrobiosis lipoidica, necrobiotic type

Systemic lupus erythematosus

Disseminated eosinophilic collagen disease

Secondary Sjögren's syndrome with multisystem involvement

Epidermolysis bullosa simplex with hypodontia

Cutis laxa secondary to inherited disorder of connective tissue

Lichen planus-lupus erythematosus overlap

Inherited disorder of connective tissue

Epidermolysis bullosa simplex

Sarcoma of connective tissue

Autoimmune connective tissue disorder

Secondary antiphospholipid syndrome

Keratoderma due to Dowling-Meara type epidermolysis bullosa simplex

Drug-induced pemphigus vulgaris

SLE glomerulonephritis syndrome, WHO class VI

Dominant dystrophic epidermolysis bullosa with absence of skin

Pemphigus erythematosus

Eosinophilia myalgia syndrome

Lupus erythematosus overlap syndrome

Congenital junctional epidermolysis bullosa

Inherited epidermolysis bullosa

Localized junctional epidermolysis bullosa

Liposarcoma of connective tissue

Junctional epidermolysis bullosa

Necrobiosis lipoidica

Epidermolysis bullosa pruriginosa

Primary Sjögren's syndrome with organ/system involvement

Idiopathic mid-dermal elastolysis

Dominant dystrophic epidermolysis bullosa

Inherited cutis laxa

Generalized recessive non-mutilating dystrophic epidermolysis bullosa

SLE glomerulonephritis syndrome, WHO class V

Generalized recessive dystrophic epidermolysis bullosa mitis

Metabolic disease of collagen

Epidermolysis bullosa simplex of the hands and feet

Lung disease with systemic lupus erythematosus

Lupus hepatitis

Necrobiosis lipoidica diabeticorum

Bullous systemic lupus erythematosus

Dermatosparaxis in cattle AND/OR sheep

Undifferentiated connective tissue disease

Epidermolysis bullosa simplex with mottled pigmentation

Cutis laxa-corneal clouding-oligophrenia syndrome

Sclerodermatomyositis

Connective tissue disease overlap syndrome

Junctional epidermolysis bullosa mitis

Drug-induced systemic lupus erythematosus

Weber-Cockayne syndrome

Nonbacterial verrucal endocardiosis

Acquired perforating pseudoxanthoma elasticum

Sjögren's syndrome

Secondary antiphospholipid syndrome with organ/system involvement

Drug-induced lupus erythematosus due to hydralazine

Dystrophic epidermolysis bullosa

Congenital junctional epidermolysis bullosa-pyloric atresia syndrome

Lymphoepithelial sialadenitis of Sjögren's syndrome

SLE glomerulonephritis syndrome, WHO class III

Systemic lupus erythematosus encephalitis

Inherited pseudoxanthoma elasticum

Pemphigus minor

Fibrosclerosis - systemic

Musculoskeletal and connective tissue disorder

Neoplasm of connective tissues

Primary Sjögren's syndrome with multisystem involvement

Hemolytic anemia with emphysema AND cutis laxa

Autosomal dominant pseudoxanthoma elasticum

Neonatal cutis laxa with marfanoid phenotype

Overlap syndrome

Lupus disease of the lung

Noninflammatory dermal elastolysis

Inverse junctional epidermolysis bullosa

Granulomatosis disciformis et progressiva

Drug-induced cutis laxa

Cutaneous asthenia in dogs AND/OR cats

Rash of systemic lupus erythematosus

Mixed collagen vascular disease

Dystrophic epidermolysis bullosa inverse type

Systemic lupus erythematosus with pericarditis

Primary antiphospholipid syndrome

Leiomyosarcoma of connective tissue

Marfan's syndrome

Eosinophilia-myalgia syndrome from tryptophan

Benign connective tissue neoplasm

Abscess of connective tissue

Pemphigus vegetans of Neumann type

Epidermolysis simplex superficialis

Cicatricial junctional epidermolysis bullosa

Epidermolysis bullosa simplex herpetiformis

Acute systemic lupus erythematosus

Drug-induced lupus erythematosus due to procainamide

Localized abdominal wall skin atrophy

Antiphospholipid syndrome

Necrobiosis lipoidica, granulomatous type

Marfanoid mental retardation syndrome

Secondary antiphospholipid syndrome with multisystem involvement

Adult junctional epidermolysis bullosa

Localized dystrophic epidermolysis bullosa

Lupus erythematosus

Cutis laxa of lower eyelid

Cutis laxa

Oral pemphigus vulgaris

Neonatal lupus erythematosus

Junctional epidermolysis bullosa gravis of Herlitz

Cutis laxa, autosomal recessive

Connective tissue disorder by body site

Dominant dystrophic epidermolysis bullosa, albopapular type

Limited lupus erythematosus

Congenital/hereditary cutis laxa

Drug-induced lupus erythematosus due to diphenylhydantoin

Secondary Sjögren's syndrome

Progressive junctional epidermolysis bullosa (neurotrophic)

Body tissue structure

1

Entire body as a whole

Tissue

T-1A200

Connective tissue structure (body structure)

Connective tissue, NOS

Connective tissue

T024

C0009780

Undifferentiated mesenchymal cell