Abnormality of the intestine

Symptom Information:

Symptom ID: HPO:0002242
Synonyms:
Enteropathy [HPO:0002242]
Enteropathy [OMIM:Enteropathy]
Quality:
Cross references:
OMIM: "Enteropathy" [OMIM:Enteropathy]
UMLS:C0021831 "Enteropathy" [HPO:0002242]
Is a (Direct Parents):
HPO         Abnormality of the gastrointestinal tract
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:
Database Frequency: 42 / 7739
Resource:

All diseases associated with this symptom:

15q24 microdeletion syndrome (Orphanet:94065)
Beh├žet 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)