Abdominal wall muscle weakness
Symptom Information:
Symptom ID: | HPO:0009023 | ||||||||||
Synonyms: |
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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 the abdomen(HPO:0001438) Abnormality of the abdominal wall(HPO:0004298) Abnormality of the abdominal musculature(HPO:0010991) Abdominal wall muscle weakness(HPO:0009023) Abnormality of the musculature(HPO:0003011) Abnormality of muscle physiology(HPO:0011804) Muscle weakness(HPO:0001324) Abdominal wall muscle weakness(HPO:0009023) MedDRA: |
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Database Frequency: | 12 / 7739 | ||||||||||
Resource: |
All diseases associated with this symptom:
Beckwith-Wiedemann syndrome due to NSD1 mutation | (Orphanet:238613) |
DIASTASIS RECTI AND WEAKNESS OF THE LINEA ALBA | (OMIM:612198) |
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1 | (OMIM:158900) |
Facioscapulohumeral dystrophy | (Orphanet:269) |
Glycogen storage disease due to acid maltase deficiency | (Orphanet:365) |
Hypocalcemic vitamin D-dependent rickets | (Orphanet:289157) |
Hypocalcemic vitamin D-resistant rickets | (Orphanet:93160) |
Leprechaunism | (Orphanet:508) |
Megacystis-microcolon-intestinal hypoperistalsis syndrome | (Orphanet:2241) |
Menkes disease | (Orphanet:565) |
Niemann-Pick disease type C | (Orphanet:646) |
Shprintzen-Goldberg syndrome | (Orphanet:2462) |