Abnormality of the musculature
Symptom Information:
| Symptom ID: | HPO:0003011 | |
| Synonyms: |
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| Quality: | ||
| Cross references: |
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| Is a (Direct Parents): | ||
| Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the musculature(HPO:0003011) MedDRA: |
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| Database Frequency: | 47 / 7739 | |
| Resource: |
All diseases associated with this symptom:
| Alveolar echinococcosis | (Orphanet:284) |
| Antecubital pterygium syndrome | (Orphanet:2987) |
| Autoimmune polyendocrinopathy type 2 | (Orphanet:3143) |
| Autosomal dominant striatal neurodegeneration | (Orphanet:228169) |
| CHROMOSOME 8q12.1-q21.2 DELETION SYNDROME | (OMIM:600257) |
| CRAMPS, FAMILIAL ADOLESCENT | (OMIM:218050) |
| Carnitine palmitoyl transferase II deficiency, myopathic form | (Orphanet:228302) |
| Congenital bile acid synthesis defect type 4 | (Orphanet:79095) |
| Congenital cataracts - facial dysmorphism - neuropathy | (Orphanet:48431) |
| Congenital contractural arachnodactyly | (Orphanet:115) |
| Congenital ichthyosis - microcephalus - tetraplegia | (Orphanet:2271) |
| Desmoid tumor | (Orphanet:873) |
| Early-onset generalized limb-onset dystonia | (Orphanet:256) |
| Encephalopathy due to hydroxykynureninuria | (Orphanet:79155) |
| Erythrokeratodermia - ataxia | (Orphanet:1955) |
| Familial leiomyomatosis | (Orphanet:523) |
| Familial partial lipodystrophy associated with PPARG mutations | (Orphanet:79083) |
| Familial partial lipodystrophy, Köbberling type | (Orphanet:79084) |
| Focal facial dermal dysplasia | (Orphanet:79133) |
| Hereditary cerebral cavernous malformation | (Orphanet:221061) |
| Hydatidosis | (Orphanet:400) |
| Infantile myofibromatosis | (Orphanet:2591) |
| Intellectual deficit, X-linked, Cantagrel type | (Orphanet:85277) |
| Lymphedema - distichiasis | (Orphanet:33001) |
| MACROCEPHALY/MEGALENCEPHALY SYNDROME, AUTOSOMAL RECESSIVE | (OMIM:248000) |
| Mandibuloacral dysplasia with type A lipodystrophy | (Orphanet:90153) |
| Metachromatic leukodystrophy | (Orphanet:512) |
| Multiple benign circumferential skin creases on limbs | (Orphanet:2505) |
| Myalgia-eosinophilia syndrome associated with tryptophan | (Orphanet:2582) |
| Netherton syndrome | (Orphanet:634) |
| Nijmegen breakage syndrome | (Orphanet:647) |
| Ophthalmoplegia - myalgia - tubular aggregates | (Orphanet:2742) |
| PERONEUS TERTIUS MUSCLE, ABSENCE OF | (OMIM:261400) |
| Pantothenate kinase-associated neurodegeneration | (Orphanet:157850) |
| Polyneuropathy - hand defect | (Orphanet:2926) |
| Primary orthostatic tremor | (Orphanet:238606) |
| Progressive hemifacial atrophy | (Orphanet:1214) |
| Progressive osseous heteroplasia | (Orphanet:2762) |
| ROWLEY-ROSENBERG SYNDROME | (OMIM:268500) |
| Radio-ulnar synostosis - intellectual deficit - hypotonia | (Orphanet:3270) |
| Sodium channelopathy-related small fiber neuropathy | (Orphanet:306577) |
| Stiff skin syndrome | (Orphanet:2833) |
| Stormorken-Sjaastad-Langslet syndrome | (Orphanet:3204) |
| Trismus - pseudocamptodactyly | (Orphanet:3377) |
| X-linked intellectual deficit with marfanoid habitus | (Orphanet:776) |
| X-linked thrombocytopenia with normal platelets | (Orphanet:852) |
| Yellow nail syndrome | (Orphanet:662) |