Diarrhea 9 - CISMeF

Preferred Label : Diarrhea 9;

Symbol : DIAR9;

CISMeF acronym : DIAR9;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal recessive;

Molecular basis : Caused by mutation in the wingless-type MMTV integration site family, member-2B gene (WNT2B, 601968.0001);

Laboratory abnormalities : Elevated fecal fat; Elevated fecal lactoferrin;

Prefixed ID : #618168;

Details

Origin ID

618168;

UMLS CUI

C4748517;

Genes related to phenotype
- Wingless-type mmtv integration site family, member 2b [OMIM gene]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Diarrhea [HPO term]
- Failure to thrive [HPO term]
- Villous atrophy [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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