Disorder of vitamin and non-protein cofactor absorption and transport

Summary

Disorder of vitamin and non-protein cofactor absorption and transport (MONDO:0017758) is a disease. A subtype of disorder of metabolite absorption and transport — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

Field	Value
Canonical name	disorder of vitamin and non-protein cofactor absorption and transport
Mondo ID	MONDO:0017758
Orphanet	309827
ICD-11	1112006621
UMLS	C5681037
MedGen	1842689
GARD	0021350
Is cancer (heuristic)	no

Also known as: disorder of vitamin and non-protein cofactor absorption and transport

Disease family

This is a subtype of disorder of metabolite absorption and transport. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by etiologic mechanism › disease of genetic or genomic mechanism › hereditary disease › inborn errors of metabolism › disorder of metabolite absorption and transport › disorder of vitamin and non-protein cofactor absorption and transport

Related subtypes (2): maternal riboflavin deficiency, disorder of mineral absorption and transport

Subtypes (4): hereditary hypercarotenemia and vitamin A deficiency, disorder of folate metabolism and transport, disorder of thiamine metabolism and transport, inborn disorder of cobalamin metabolism and transport

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

No druggable-target or therapeutic data for this disease’s cohort.

Clinical trials & evidence

Clinical trials

Clinical trials: 0.