Aplasia/Hypoplasia of the abdominal wall musculature

Symptom Information:

Symptom ID: HPO:0010318
Abdominal wall muscle hypoplasia [Orphanet:17440]
Abdominal wall muscle absence [Orphanet:17440]
Absent/hypotonic/flaccid abdominal wall muscles [Orphanet:17440]
Cross references:
HPO:0005247 "Hypoplasia of the abdominal wall musculature" [Orphanet:17440]
HPO:0005199 "Aplasia of the abdominal wall musculature" [Orphanet:17440]
Orphanet:17440 "Absent/hypotonic/flaccid abdominal wall muscles" [Orphanet:17440]
Is a (Direct Parents):
Orphanet Aplasia of the abdominal wall musculature
HPO         Abnormality of the abdominal musculature
Orphanet Abnormality of the abdominal wall
Is a (Whole tree): HPO:
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the abdomen(HPO:0001438)
          Abnormality of the abdominal wall(HPO:0004298)
             Abnormality of the abdominal musculature(HPO:0010991)
                Aplasia/Hypoplasia of the abdominal wall musculature(HPO:0010318)
Database Frequency: 55 / 7739

All diseases associated with this symptom:

Athyreosis (Orphanet:95713)
Autosomal recessive multiple pterygium syndrome (Orphanet:2990)
Beta-mannosidosis (Orphanet:118)
Boomerang dysplasia (Orphanet:1263)
C syndrome (Orphanet:1308)
CEDNIK syndrome (Orphanet:66631)
Cartilage-hair hypoplasia (Orphanet:175)
Central congenital hypothyroidism (Orphanet:226298)
Congenital hypothyroidism (Orphanet:442)
Congenital hypothyroidism due to developmental anomaly (Orphanet:95711)
Congenital hypothyroidism due to transplacental passage of maternal TSH-binding inhibitory antibodies (Orphanet:95715)
Cutis laxa (Orphanet:209)
De Barsy syndrome (Orphanet:2962)
Desbuquois syndrome (Orphanet:1425)
Diabetic embryopathy (Orphanet:1926)
Ehlers-Danlos syndrome, classic type (Orphanet:287)
Ehlers-Danlos syndrome, hypermobility type (Orphanet:285)
Ehlers-Danlos syndrome, progeroid type (Orphanet:75496)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Familial thyroid dyshormonogenesis (Orphanet:95716)
Familial visceral myopathy (Orphanet:2604)
Free sialic acid storage disease (Orphanet:834)
GM1 gangliosidosis (Orphanet:354)
Glycogen storage disease due to acid maltase deficiency (Orphanet:365)
Hyposmia - nasal and ocular hypoplasia - hypogonadotropic hypogonadism (Orphanet:2250)
Hypothyroidism due to TSH receptor mutations (Orphanet:90673)
Hypothyroidism due to deficient transcription factors involved in pituitary development or function (Orphanet:226307)
Idiopathic congenital hypothyroidism (Orphanet:95717)
Infantile neuronal ceroid lipofuscinosis (Orphanet:79263)
Isolated thyroid-stimulating hormone deficiency (Orphanet:90674)
Krabbe disease (Orphanet:487)
Late infantile neuronal ceroid lipofuscinosis (Orphanet:168491)
Leprechaunism (Orphanet:508)
McDonough syndrome (Orphanet:2471)
Menkes disease (Orphanet:565)
Mucolipidosis type 4 (Orphanet:578)
Neurofibromatosis - Noonan syndrome (Orphanet:638)
Niemann-Pick disease type C (Orphanet:646)
Noonan syndrome (Orphanet:648)
Noonan syndrome with multiple lentigines (Orphanet:500)
Peripheral hypothyroidism (Orphanet:226310)
Peripheral resistance to thyroid hormones (Orphanet:97927)
Permanent congenital hypothyroidism (Orphanet:226292)
Primary congenital hypothyroidism (Orphanet:226295)
Primary congenital hypothyroidism without thyroid developmental anomaly (Orphanet:95714)
Prune belly syndrome (Orphanet:2970)
Resistance to thyrotropin-releasing hormone syndrome (Orphanet:99832)
Rheumatic fever (Orphanet:3099)
SCARF syndrome (Orphanet:3134)
Shprintzen-Goldberg syndrome (Orphanet:2462)
Sialidosis type 2 (Orphanet:87876)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Thyroid ectopia (Orphanet:95712)
Thyroid hemiagenesis (Orphanet:95719)
Thyroid hypoplasia (Orphanet:95720)