Q79.6 Dermatosparaxis

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Dermatosparaxis

Dermatosparaxis
Synonym for Ehlers-Danlos syndrome

    Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)|Q65-Q79 Congenital malformations and deformations of the musculoskeletal system (Q65-Q79)|Q79 Congenital malformations of musculoskeletal system, not elsewhere classified

Results for Dermatosparaxis and additional synonyms


Q79.6
Ehlers-Danlos syndrome

Synonyms:

Arthrochalasia multiplex congenita|Arthrochalasis multiplex congenita|Benign hypermobility syndrome|Corneal fragility keratoglobus, blue sclerae AND joint hypermobility|Corneal fragility keratoglobus, blue sclerae AND joint hypermobility (disorder)|Cutis elastica|Cutis hyperelastica|Cutis hyperelastica dermatorrhexis|Cutis laxa, X-linked|Cutis laxa, x-linked|Cutis laxa, x-linked (disorder)|Danlos disease|Dermatorrhexis with dermatochalasis AND arthrochalasis|Dermatosparaxis|Dystrophia mesodermalis congenita|Ehlers-Danlos syndrome (disorder)|Ehlers-Danlos syndrome Type VI - ocular (recessive)|Ehlers-Danlos syndrome arterial type E-D|Ehlers-Danlos syndrome ecchymotic type E-D|Ehlers-Danlos syndrome type 7|Ehlers-Danlos syndrome type 8|Ehlers-Danlos syndrome type 9 X-linked|Ehlers-Danlos syndrome type I|Ehlers-Danlos syndrome type II|Ehlers-Danlos syndrome type III|Ehlers-Danlos syndrome type IV|Ehlers-Danlos syndrome type V|Ehlers-Danlos syndrome type VI|Ehlers-Danlos syndrome type VIII|Ehlers-Danlos syndrome type XI|Ehlers-Danlos syndrome with platelet dysfunction|Ehlers-Danlos syndrome, autosomal dominant type 7|Ehlers-Danlos syndrome, autosomal recessive type 7|Ehlers-Danlos syndrome, benign hypermobile form|Ehlers-Danlos syndrome, dominant type 4|Ehlers-Danlos syndrome, dominant type 4 (disorder)|Ehlers-Danlos syndrome, dysfibronectinaemic|Ehlers-Danlos syndrome, dysfibronectinemic|Ehlers-Danlos syndrome, dysfibronectinemic (disorder)|Ehlers-Danlos syndrome, familial joint laxity type|Ehlers-Danlos syndrome, familial joint laxity type (disorder)|Ehlers-Danlos syndrome, gravis|Ehlers-Danlos syndrome, hydroxylysine-deficient|Ehlers-Danlos syndrome, hydroxylysine-deficient (disorder)|Ehlers-Danlos syndrome, lysyl hydroxylase deficient|Ehlers-Danlos syndrome, mental retardation type|Ehlers-Danlos syndrome, mild classic form|Ehlers-Danlos syndrome, mild x-linked|Ehlers-Danlos syndrome, mitis|Ehlers-Danlos syndrome, mutant procollagen type 7|Ehlers-Danlos syndrome, non hydroxylysine deficient ocular type|Ehlers-Danlos syndrome, non hydroxylysine deficient ocular type (disorder)|Ehlers-Danlos syndrome, occipital horn type|Ehlers-Danlos syndrome, periodontitis type|Ehlers-Danlos syndrome, procollagen proteinase deficient|Ehlers-Danlos syndrome, procollagen proteinase deficient (disorder)|Ehlers-Danlos syndrome, procollagen proteinase resistant|Ehlers-Danlos syndrome, procollagen proteinase resistant (disorder)|Ehlers-Danlos syndrome, recessive type 4|Ehlers-Danlos syndrome, recessive type 4 (disorder)|Ehlers-Danlos syndrome, severe classic form|Ehlers-Danlos syndrome, type 1|Ehlers-Danlos syndrome, type 1 (disorder)|Ehlers-Danlos syndrome, type 10|Ehlers-Danlos syndrome, type 11|Ehlers-Danlos syndrome, type 2|Ehlers-Danlos syndrome, type 2 (disorder)|Ehlers-Danlos syndrome, type 3|Ehlers-Danlos syndrome, type 3 (disorder)|Ehlers-Danlos syndrome, type 4|Ehlers-Danlos syndrome, type 4 (disorder)|Ehlers-Danlos syndrome, type 5|Ehlers-Danlos syndrome, type 5 (disorder)|Ehlers-Danlos syndrome, type 6 phenotype with macrocephaly|Ehlers-Danlos syndrome, type 8|Ehlers-Danlos syndrome, type 8 (disorder)|Ehlers-Danlos syndrome, type 9|Ehlers-Danlos syndrome, x-linked skeletal type|Familial generalised articular hypermobility|Familial generalized articular hypermobility|Familial joint instability syndrome|Familial joint laxity|Fibrodysplasia elastica generalisata|Fragilitas oculi with joint hyperextensibility|Hereditary collagen dysplasia|Hydroxylysine-deficient collagen disease|India rubber skin|Kyphoscoliosis type|Meekeren-Ehlers-Danlos syndrome|Occipital horn syndrome|Periodontitis associated with Ehlers-Danlos syndrome type VIII|Procollagen aminoprotease deficiency|Procollagen peptidase deficiency|Procollagen protease deficiency|Protocollagen lysyl hydroxylase deficiency|Sack syndrome|Sack-Barabas syndrome

Subcategories:

    All content of the ICD-10 CM Search is based on the classifications and codes of the Centers for Medicare and Medicaid Services (CMS) and the National Center for Health Statistics (NCHS). The accumulation of synonyms is carried out by Averbis GmbH with Healthcare Natural Language Processing. All information is provided without guarantee. Errors and omissions excepted. We expressly reserve the right to make changes, additions or deletions to the information or links provided at any time without prior notice. Our offer is non-binding. For correctness, completeness and topicality or designations no liability is assumed.

    ICD-Search ICD 10 CM (Clinical Modification) 2017 through Healthcare Natural Language Processing & Deep Learning

    ICD-Code / International Statistical Classification of Diseases and Related Health Problems (ICD) for: Dermatosparaxis

    ICD Code for Disease, Diagnosis Q79.6

    ICD Code an Classification Ehlers-Danlos syndrome

    Chapter, Outline, Main Categories, Parent Concepts or Top Concepts: Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)|Q65-Q79 Congenital malformations and deformations of the musculoskeletal system (Q65-Q79)|Q79 Congenital malformations of musculoskeletal system, not elsewhere classified

    Subcategories, subconcepts or child concepts:

    Synonyms:

    Synonyms: Q79.6: Dermatosparaxis

    Other Synonyms of the Category: Arthrochalasia multiplex congenita|Arthrochalasis multiplex congenita|Benign hypermobility syndrome|Corneal fragility keratoglobus, blue sclerae AND joint hypermobility|Corneal fragility keratoglobus, blue sclerae AND joint hypermobility (disorder)|Cutis elastica|Cutis hyperelastica|Cutis hyperelastica dermatorrhexis|Cutis laxa, X-linked|Cutis laxa, x-linked|Cutis laxa, x-linked (disorder)|Danlos disease|Dermatorrhexis with dermatochalasis AND arthrochalasis|Dermatosparaxis|Dystrophia mesodermalis congenita|Ehlers-Danlos syndrome (disorder)|Ehlers-Danlos syndrome Type VI - ocular (recessive)|Ehlers-Danlos syndrome arterial type E-D|Ehlers-Danlos syndrome ecchymotic type E-D|Ehlers-Danlos syndrome type 7|Ehlers-Danlos syndrome type 8|Ehlers-Danlos syndrome type 9 X-linked|Ehlers-Danlos syndrome type I|Ehlers-Danlos syndrome type II|Ehlers-Danlos syndrome type III|Ehlers-Danlos syndrome type IV|Ehlers-Danlos syndrome type V|Ehlers-Danlos syndrome type VI|Ehlers-Danlos syndrome type VIII|Ehlers-Danlos syndrome type XI|Ehlers-Danlos syndrome with platelet dysfunction|Ehlers-Danlos syndrome, autosomal dominant type 7|Ehlers-Danlos syndrome, autosomal recessive type 7|Ehlers-Danlos syndrome, benign hypermobile form|Ehlers-Danlos syndrome, dominant type 4|Ehlers-Danlos syndrome, dominant type 4 (disorder)|Ehlers-Danlos syndrome, dysfibronectinaemic|Ehlers-Danlos syndrome, dysfibronectinemic|Ehlers-Danlos syndrome, dysfibronectinemic (disorder)|Ehlers-Danlos syndrome, familial joint laxity type|Ehlers-Danlos syndrome, familial joint laxity type (disorder)|Ehlers-Danlos syndrome, gravis|Ehlers-Danlos syndrome, hydroxylysine-deficient|Ehlers-Danlos syndrome, hydroxylysine-deficient (disorder)|Ehlers-Danlos syndrome, lysyl hydroxylase deficient|Ehlers-Danlos syndrome, mental retardation type|Ehlers-Danlos syndrome, mild classic form|Ehlers-Danlos syndrome, mild x-linked|Ehlers-Danlos syndrome, mitis|Ehlers-Danlos syndrome, mutant procollagen type 7|Ehlers-Danlos syndrome, non hydroxylysine deficient ocular type|Ehlers-Danlos syndrome, non hydroxylysine deficient ocular type (disorder)|Ehlers-Danlos syndrome, occipital horn type|Ehlers-Danlos syndrome, periodontitis type|Ehlers-Danlos syndrome, procollagen proteinase deficient|Ehlers-Danlos syndrome, procollagen proteinase deficient (disorder)|Ehlers-Danlos syndrome, procollagen proteinase resistant|Ehlers-Danlos syndrome, procollagen proteinase resistant (disorder)|Ehlers-Danlos syndrome, recessive type 4|Ehlers-Danlos syndrome, recessive type 4 (disorder)|Ehlers-Danlos syndrome, severe classic form|Ehlers-Danlos syndrome, type 1|Ehlers-Danlos syndrome, type 1 (disorder)|Ehlers-Danlos syndrome, type 10|Ehlers-Danlos syndrome, type 11|Ehlers-Danlos syndrome, type 2|Ehlers-Danlos syndrome, type 2 (disorder)|Ehlers-Danlos syndrome, type 3|Ehlers-Danlos syndrome, type 3 (disorder)|Ehlers-Danlos syndrome, type 4|Ehlers-Danlos syndrome, type 4 (disorder)|Ehlers-Danlos syndrome, type 5|Ehlers-Danlos syndrome, type 5 (disorder)|Ehlers-Danlos syndrome, type 6 phenotype with macrocephaly|Ehlers-Danlos syndrome, type 8|Ehlers-Danlos syndrome, type 8 (disorder)|Ehlers-Danlos syndrome, type 9|Ehlers-Danlos syndrome, x-linked skeletal type|Familial generalised articular hypermobility|Familial generalized articular hypermobility|Familial joint instability syndrome|Familial joint laxity|Fibrodysplasia elastica generalisata|Fragilitas oculi with joint hyperextensibility|Hereditary collagen dysplasia|Hydroxylysine-deficient collagen disease|India rubber skin|Kyphoscoliosis type|Meekeren-Ehlers-Danlos syndrome|Occipital horn syndrome|Periodontitis associated with Ehlers-Danlos syndrome type VIII|Procollagen aminoprotease deficiency|Procollagen peptidase deficiency|Procollagen protease deficiency|Protocollagen lysyl hydroxylase deficiency|Sack syndrome|Sack-Barabas syndrome

    ICD 10 CM 2017, (Clinical Modification) for coding of death certificates and mortality data. The international Statistical Classification of Diseases and Related Health Problems (ICD) 10th Revision and Clinical Modification. International Classification of Diseases, Tenth Revision, Clinical Modification.Q79.6 Ehlers-Danlos syndrome and Dermatosparaxis

    Dermatosparaxis
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