Abnormality of the musculature

Symptom Information:

Symptom ID: HPO:0003011
Synonyms:
Muscular abnormality [HPO:0003011]
Quality:
Cross references:
Is a (Direct Parents):
HPO         Phenotypic abnormality
HPO         Abnormality of musculature of pharynx
HPO         Abnormality of occipitofrontalis muscle
HPO         Abnormality of hyoglossus muscle
HPO         Abnormality of the tongue muscle
HPO         Abnormality of lateral crico-arytenoid
HPO         Abnormality of musculature of soft palate
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the musculature(HPO:0003011)
MedDRA:
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)