Increased connective tissue
Symptom Information:
Symptom ID: | HPO:0009025 | ||
Synonyms: |
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Quality: | |||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of connective tissue(HPO:0003549) Increased connective tissue(HPO:0009025) MedDRA: |
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Database Frequency: | 11 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal dominant Charcot-Marie-Tooth disease type 2E | (Orphanet:99939) |
Autosomal dominant limb-girdle muscular dystrophy type 1F | (Orphanet:55595) |
Autosomal dominant limb-girdle muscular dystrophy type 1H | (Orphanet:238755) |
Autosomal recessive limb-girdle muscular dystrophy type 2B | (Orphanet:268) |
Autosomal recessive limb-girdle muscular dystrophy type 2G | (Orphanet:34514) |
Congenital multicore myopathy with external ophthalmoplegia | (Orphanet:98905) |
Ehlers-Danlos syndrome due to tenascin-X deficiency | (Orphanet:230839) |
Epidermolysis bullosa simplex with muscular dystrophy | (Orphanet:257) |
Myosclerosis | (Orphanet:289380) |
Pearson syndrome | (Orphanet:699) |
Severe X-linked mitochondrial encephalomyopathy | (Orphanet:238329) |