Peripheral resistance to thyroid hormones

Summary

Peripheral resistance to thyroid hormones (MONDO:0019995) is a disease. A subtype of peripheral hypothyroidism — 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	peripheral resistance to thyroid hormones
Mondo ID	MONDO:0019995
Orphanet	97927
SNOMED CT	718193005
UMLS	C4273673
MedGen	902322
GARD	0012734
Is cancer (heuristic)	no

Disease family

This is a subtype of peripheral hypothyroidism. 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 body system or component › endocrine system disorder › hereditary endocrine growth disease › permanent congenital hypothyroidism › peripheral hypothyroidism › peripheral resistance to thyroid hormones

Related subtypes (1): thyroid hormone metabolism, abnormal 1

Subtypes (2): congenital nongoitrous hypothyroidism 3, congenital nongoitrous hypothyroidism 6

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.