Abdominal wall muscle weakness

Symptom Information:

Symptom ID: HPO:0009023
Synonyms:
Lax abdominal musculature [HPO:0009023]
Abdominal wall muscle hypotonia [Orphanet:17440]
Abdominal weakness (finding) [Orphanet:17440]
Abdominal weakness [Orphanet:17440]
Lax abdominal musculature [OMIM:Lax abdominal musculature]
Absent/hypotonic/flaccid abdominal wall muscles [Orphanet:17440]
Abdominal wall muscle weakness (later onset) [OMIM:Abdominal wall muscle weakness (later onset)]
Quality:
Cross references:
Orphanet:17440 "Absent/hypotonic/flaccid abdominal wall muscles" [Orphanet:17440]
OMIM: "Lax abdominal musculature" [OMIM:Lax abdominal musculature]
OMIM: "Abdominal wall muscle weakness (later onset)" [OMIM:Abdominal wall muscle weakness (later onset)]
UMLS:C0581877 "Abdominal weakness" [Orphanet:17440]
Is a (Direct Parents):
HPO         Muscle weakness
HPO         Abnormality of the abdominal musculature
Orphanet Aplasia of the abdominal wall musculature
Orphanet Abnormality of the abdominal wall
HPO         Beevor's sign
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:
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)