Atrophy
Symptom Information:
Symptom ID: | MedDRA:10003694 | ||
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:
MedDRA: General disorders and administration site conditions(MedDRA:10018065) Tissue disorders NEC(MedDRA:10007867) Trophic disorders(MedDRA:10044694) Atrophy(MedDRA:10003694) |
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Database Frequency: | 7 / 7739 | ||
Resource: |
All diseases associated with this symptom:
3-@METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY | (OMIM:210210) |
Arthrogryposis-like syndrome | (Orphanet:1149) |
COCKAYNE SYNDROME A | (OMIM:216400) |
COCKAYNE SYNDROME B | (OMIM:133540) |
COCKAYNE SYNDROME, TYPE III | (OMIM:216411) |
SPINOCEREBELLAR ATAXIA WITH RIGIDITY AND PERIPHERAL NEUROPATHY | (OMIM:183050) |
Spastic paraplegia type 2 | (Orphanet:99015) |