Froelich syndrome

disease
On this page

Also known as Adiposodysgenesisadiposogenital dystrophyBabinski-Froelich syndromedystrophia AdiposogenitalisFroehlich's syndromeFroelich's adiposityFroelich's syndromeFrohlich syndromeFrohlich's syndromeFrolich's syndromeFröhlich syndromehypothalamic infantilism-obesityLaunois-Cleret syndromesexual infantilism

Summary

Froelich syndrome (MONDO:0003962) is a disease. A subtype of hypothalamic disorder — 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

FieldValue
Canonical nameFroelich syndrome
Mondo IDMONDO:0003962
DOIDDOID:6676
NCITC34625
SNOMED CT62999006
UMLSC0016724
MedGen4795
Is cancer (heuristic)no

Also known as: Adiposodysgenesis · adiposogenital dystrophy · Babinski-Froelich syndrome · dystrophia Adiposogenitalis · Froehlich’s syndrome · Froelich’s adiposity · Froelich’s syndrome · Frohlich syndrome · Frohlich’s syndrome · Frolich’s syndrome · Fröhlich syndrome · hypothalamic infantilism-obesity · Launois-Cleret syndrome · sexual infantilism

Disease family

Classification path: disease › human disease › disease by body system or component › nervous system disordercentral nervous system disorderbrain disorder › thalamic disorder › hypothalamic disorder › Froelich syndrome

Related subtypes (2): hypothalamic neoplasm, hypothalamic dysfunction

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.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.