AlternativeMed
modern wellness Β· Symptom

Chronic diarrhea

🩺 HPO Source
HPO Label
Chronic diarrhea
HPO Definition
The presence of chronic diarrhea, which is usually taken to mean diarrhea that has persisted for over 4 weeks.
πŸ”€ Synonyms (5)
Synonyms
Chronic diarrheaChronic diarrhoeaDiarrhea, recurrentRecurrent diarrheaRecurrent diarrhoea
πŸ”— Cross-References (2)
SNOMEDCT_US236071009
UMLSC0401151
πŸ”Ό Broader Terms (1)
HP:0002014Diarrhea
πŸ₯ Conditions where Chronic diarrhea appears
40 Β· bridged via HPO ↔ OMIM
syndrome OMIM 615873
Adnp-Related Multiple Congenital Anomalies, Intellectual Disability, Autism Spectrum Disorder
freq: 1/10 ev: PCS
syndrome OMIM 601495
Agammaglobulinemia 1, Autosomal Recessive
freq: 4/19 ev: PCS
syndrome OMIM 208900
Ataxia Telangiectasia
freq: 1/2 ev: PCS
syndrome OMIM 208900
Ataxia-Telangiectasia Variant
freq: 1/2 ev: PCS
syndrome OMIM 602450
Athabaskan Severe Combined Immunodeficiency
freq: 1/1 ev: PCS
syndrome OMIM 613385
Autoimmune Disease, Multisystem, With Facial Dysmorphism
freq: 3/11 ev: PCS
syndrome OMIM 607271
Autoimmune Lymphoproliferative Syndrome Type 2B
freq: 1/2 ev: PCS
syndrome OMIM 613291
Bile Acid Malabsorption, Primary
freq: 1/1 onset: HP:0003623 ev: PCS
disease OMIM 242700
Congenital Absence of Thymus
ev: IEA
syndrome OMIM 613489
Congenital Disorder of Glycosylation, Type Iij
freq: HP:0040283 ev: TAS
syndrome OMIM 614576
Congenital Disorder of Glycosylation, Type Iil
freq: 3/5 ev: PCS
syndrome OMIM 606824
Congenital Glucose-Galactose Malabsorption
freq: 2/2 ev: PCS
disease OMIM 304150
Cutis Laxa, X-Linked
freq: 3/4 ev: IEA
syndrome OMIM 614379
Decreased Serum Complement C4B
freq: 1/1 onset: HP:0003593 ev: PCS
syndrome OMIM 614616
Diarrhea 6
freq: 32/32 ev: PCS
syndrome OMIM 223370
Dubowitz Syndrome
ev: IEA
syndrome OMIM 613989
Dyskeratosis Congenita, Autosomal Dominant 2
ev: TAS
syndrome OMIM 612132
Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant
freq: 1/1 onset: HP:0003593 ev: PCS
syndrome OMIM 602473
Ethylmalonic Encephalopathy
freq: 6/8 ev: PCS
syndrome OMIM 614921
Glycogen Storage Disease Xiv
freq: 2/11 ev: PCS
syndrome OMIM 233600
Granulocytopenia With Immunoglobulin Abnormality
freq: 1/1 ev: PCS
syndrome OMIM 260920
Hyperimmunoglobulinemia D
freq: 44/60 ev: PCS
syndrome OMIM 256500
Ichthyosis Linearis Circumflexa
freq: 7/21 ev: PCS
syndrome OMIM 612782
Immune Dysfunction With T-Cell Inactivation Due To Calcium Entry Defect 1
freq: 3/6 ev: PCS
syndrome OMIM 617638
Immunodeficiency 11B With Atopic Dermatitis
freq: 1/8 ev: PCS
syndrome OMIM 615592
Immunodeficiency 15B
ev: PCS
syndrome OMIM 615607
Immunodeficiency 17
freq: 2/2 ev: PCS
syndrome OMIM 615617
Immunodeficiency 19
freq: 1/3 ev: PCS
syndrome OMIM 616005
Immunodeficiency 36
freq: HP:0040284 ev: IEA
syndrome OMIM 616433
Immunodeficiency 40
freq: 1/5 ev: PCS
syndrome OMIM 616740
Immunodeficiency 46
freq: 10/14 ev: PCS
syndrome OMIM 300972
Immunodeficiency 47
freq: 1/1 ev: PCS
syndrome OMIM 615207
Immunodeficiency 56
freq: 2/4 ev: PCS
syndrome OMIM 618131
Immunodeficiency 58
freq: 4/15 ev: PCS
syndrome OMIM 617765
Immunodeficiency, Common Variable, 14
freq: 1/3 ev: PCS
syndrome OMIM 614699
Immunodeficiency, Common Variable, 7
freq: 1/1 ev: PCS
syndrome OMIM 614700
Immunodeficiency, Common Variable, 8, With Autoimmunity
freq: 7/11 ev: PCS
syndrome OMIM 304790
Insulin-Dependent Diabetes Mellitus Secretory Diarrhea Syndrome
freq: 28/28 ev: PCS
syndrome OMIM 606367
Interleukin 2 Receptor, Alpha, Deficiency Of
freq: 1/1 onset: HP:0003593 ev: PCS
syndrome OMIM 606367
Interleukin 2 Receptor, Alpha, Deficiency Of
freq: 1/1 ev: PCS
πŸ“œ Formulas studied for Chronic diarrhea
6 Β· text-bridged via indications + syndromes