Aplasia/Hypoplasia of the abdominal wall musculature
Symptom Information:
Symptom ID: | HPO:0010318 | ||||||
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) Aplasia/Hypoplasia of the abdominal wall musculature(HPO:0010318) MedDRA: |
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Database Frequency: | 55 / 7739 | ||||||
Resource: |
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) |