Abnormality of the abdomen
Symptom Information:
| Symptom ID: | HPO:0001438 | ||
| Synonyms: |
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| Quality: | |||
| 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) MedDRA: |
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| Database Frequency: | 28 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS | (OMIM:201750) |
| Acro-oto-ocular syndrome | (Orphanet:2980) |
| BERNARD-SOULIER SYNDROME | (OMIM:231200) |
| Birt-Hogg-Dube syndrome | (Orphanet:122) |
| Blue diaper syndrome | (Orphanet:94086) |
| CORTICOTROPIN-RELEASING HORMONE | (OMIM:122560) |
| CREST syndrome | (Orphanet:90290) |
| Constitutional mismatch repair deficiency syndrome | (Orphanet:252202) |
| Cooper-Jabs syndrome | (Orphanet:1488) |
| EHLERS-DANLOS SYNDROME, AUTOSOMAL DOMINANT, TYPE UNSPECIFIED | (OMIM:130090) |
| Familial amyloidosis, Finnish type | (Orphanet:85448) |
| Fetal akinesia deformation sequence | (Orphanet:994) |
| GALLBLADDER, AGENESIS OF | (OMIM:137040) |
| GASTRIC SNEEZING | (OMIM:137130) |
| GRAVES DISEASE, SUSCEPTIBILITY TO, 1 | (OMIM:275000) |
| Hereditary hypophosphatemic rickets with hypercalciuria | (Orphanet:157215) |
| Hereditary mixed polyposis syndrome | (Orphanet:157794) |
| ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 4A | (OMIM:601277) |
| Juberg-Hayward syndrome | (Orphanet:2319) |
| METHANE PRODUCTION | (OMIM:250650) |
| Mendelian susceptibility to mycobacterial diseases | (Orphanet:748) |
| Mesomelia-synostoses syndrome | (Orphanet:2496) |
| Mucolipidosis type 4 | (Orphanet:578) |
| PELVIC LIPOMATOSIS WITH CROSSED RENAL ECTOPIA | (OMIM:169545) |
| Pancreatic beta cell agenesis with neonatal diabetes mellitus | (Orphanet:28455) |
| Parana hard-skin syndrome | (Orphanet:2812) |
| TERATOMA, PINEAL | (OMIM:273120) |
| Xq27.3q28 duplication syndrome | (Orphanet:261483) |