Diastasis recti
Symptom Information:
| Symptom ID: | HPO:0001540 | ||
| 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) Diastasis recti(HPO:0001540) MedDRA: |
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| Database Frequency: | 23 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| 3MC SYNDROME 2 | (OMIM:265050) |
| Autosomal dominant Opitz G/BBB syndrome | (Orphanet:306588) |
| Beckwith-Wiedemann syndrome | (Orphanet:116) |
| Beckwith-Wiedemann syndrome due to 11p15 microdeletion | (Orphanet:231127) |
| Beckwith-Wiedemann syndrome due to CDKN1C mutation | (Orphanet:231120) |
| Beckwith-Wiedemann syndrome due to imprinting defect of 11p15 | (Orphanet:231117) |
| Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11 | (Orphanet:96193) |
| DIASTASIS RECTI AND WEAKNESS OF THE LINEA ALBA | (OMIM:612198) |
| EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1 | (OMIM:601776) |
| Ehlers-Danlos syndrome, musculocontractural type | (Orphanet:2953) |
| Focal dermal hypoplasia | (Orphanet:2092) |
| Hurler syndrome | (Orphanet:93473) |
| Hurler-Scheie syndrome | (Orphanet:93476) |
| Isolated sedoheptulokinase deficiency | (ORPHA:440713) |
| KAGAMI-OGATA SYNDROME | (OMIM:608149) |
| McDonough syndrome | (Orphanet:2471) |
| Monosomy 5p | (Orphanet:281) |
| Mucolipidosis type 2 | (Orphanet:576) |
| Opitz G/BBB syndrome | (Orphanet:2745) |
| Peters-plus syndrome | (Orphanet:709) |
| SCARF syndrome | (Orphanet:3134) |
| Simpson-Golabi-Behmel syndrome | (Orphanet:373) |
| Weaver syndrome | (Orphanet:3447) |