Abnormality of the intestine
Symptom Information:
Symptom ID: | HPO:0002242 | ||
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) Abnormality of the abdominal organs(HPO:0002012) Abnormality of the gastrointestinal tract(HPO:0011024) Abnormality of the intestine(HPO:0002242) MedDRA: |
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Database Frequency: | 42 / 7739 | ||
Resource: |
All diseases associated with this symptom:
15q24 microdeletion syndrome | (Orphanet:94065) |
Behçet disease | (Orphanet:117) |
Blue rubber bleb nevus | (Orphanet:1059) |
Campomelia, Cumming type | (Orphanet:1318) |
Carney-Stratakis syndrome | (Orphanet:97286) |
Cholestasis - pigmentary retinopathy - cleft palate | (Orphanet:1415) |
Cocaine embryofetopathy | (Orphanet:1911) |
Colonic atresia | (Orphanet:1198) |
Cryoglobulinemic vasculitis | (Orphanet:91138) |
ENTEROPATHY, FAMILIAL, WITH VILLOUS EDEMA AND IMMUNOGLOBULIN G2 DEFICIENCY | (OMIM:600351) |
ENTEROPATHY, PROTEIN-LOSING | (OMIM:226300) |
Ehlers-Danlos syndrome, vascular type | (Orphanet:286) |
Eosinophilic granulomatosis with polyangiitis | (Orphanet:183) |
Gastrointestinal stromal tumor | (Orphanet:44890) |
Gastroschisis | (Orphanet:2368) |
Granulomatosis with polyangiitis | (Orphanet:900) |
HOMOZYGOUS 11p15-p14 DELETION SYNDROME | (OMIM:606528) |
Hereditary nonpolyposis colon cancer | (Orphanet:144) |
Hirschsprung disease | (Orphanet:388) |
Holoprosencephaly | (Orphanet:2162) |
Hypoglossia - hypodactyly | (Orphanet:989) |
IMMUNODEFICIENCY 17 | (OMIM:615607) |
Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome | (Orphanet:37042) |
Immunoglobulin A vasculitis | (Orphanet:761) |
Jervell and Lange-Nielsen syndrome | (Orphanet:90647) |
Laryngo-tracheo-esophageal cleft - pulmonary hypoplasia | (Orphanet:2005) |
Lyell syndrome | (Orphanet:537) |
MEDNIK syndrome | (Orphanet:171851) |
Malignant atrophic papulosis | (Orphanet:679) |
Marshall syndrome with periodic fever | (Orphanet:42642) |
Microscopic polyangiitis | (Orphanet:727) |
Microvillous inclusion disease | (Orphanet:2290) |
Multiple intestinal atresia | (Orphanet:2300) |
Neurogenic arthrogryposis multiplex congenita | (Orphanet:1143) |
Polyarteritis nodosa | (Orphanet:767) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Polymyositis | (Orphanet:732) |
Prune belly syndrome | (Orphanet:2970) |
Stevens-Johnson syndrome | (Orphanet:36426) |
Typhoid | (Orphanet:99745) |
Umbilical cord ulceration - intestinal atresia | (Orphanet:3405) |
ZINC DEFICIENCY, TRANSIENT NEONATAL | (OMIM:608118) |