modern wellness · Symptom
Truncal obesity
🩺 HPO Source
HPO ID
HPO Label
Truncal obesity
HPO Definition
Obesity located preferentially in the trunk of the body as opposed to the extremities.
🔤 Synonyms (2)
Synonyms
Centripetal obesityTruncal obesity
🔗 Cross-References (2)
SNOMEDCT_US248311001
UMLSC0311277
🔼 Broader Terms (1)
HP:0001513Obesity
🏥 Conditions where Truncal obesity appears
29 · bridged via HPO ↔ OMIM
syndrome OMIM 615812
Abdominal Obesity-Metabolic Syndrome 3
ev: PCS
syndrome OMIM 219080
Acth-Independent Macronodular Adrenal Hyperplasia
ev: IEA
syndrome OMIM 615873
Adnp-Related Multiple Congenital Anomalies, Intellectual Disability, Autism Spectrum Disorder
freq: 2/10 ev: PCS
syndrome OMIM 203800
Alstrom Syndrome
ev: IEA
syndrome OMIM 209900
Bardet-Biedl Syndrome 1 (Disorder)
freq: 18/22 ev: PCS
syndrome OMIM 615986
Bardet-Biedl Syndrome 9
freq: 1/1 ev: PCS
phenotype OMIM 612474
Chromosome 1Q21.1 Deletion Syndrome, 1.35-Mb
freq: 1/21 ev: PCS
disease OMIM 216550
Cohen Syndrome
freq: 1/1 ev: PCS
syndrome OMIM 300882
Cornelia De Lange Syndrome 5
ev: TAS
syndrome OMIM 615777
Desbuquois Dysplasia 2
freq: 2/7 ev: PCS
syndrome OMIM 240900
Hypoinsulinemic Hypoglycemia With Hemihypertrophy
ev: TAS
syndrome OMIM 618160
Isolated Growth Hormone Deficiency, Type V
ev: IEA
syndrome OMIM 222700
Lysinuric Protein Intolerance
ev: TAS
syndrome OMIM 613192
Mental Retardation, Autosomal Recessive 13
freq: 3/3 ev: PCS
syndrome OMIM 614202
Mental Retardation, Autosomal Recessive 15
freq: 15/19 ev: PCS
syndrome OMIM 300957
Mental Retardation, X-Linked 12
freq: 10/38 ev: PCS
syndrome OMIM 300957
Mental Retardation, X-Linked 35
freq: 10/38 ev: PCS
disease OMIM 210720
Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii
ev: IEA
syndrome OMIM 610156
Morm Syndrome
onset: HP:0011463 ev: PCS
syndrome OMIM 610489
Pigmented Nodular Adrenocortical Disease, Primary, 1 (Disorder)
ev: IEA
syndrome OMIM 610475
Pigmented Nodular Adrenocortical Disease, Primary, 2
ev: IEA
syndrome OMIM 259050
Primrose Syndrome
freq: 5/8 ev: PCS
syndrome OMIM 270450
Resistance To Insulin-Like Growth Factor I
ev: IEA
syndrome OMIM 617547
Retinal Dystrophy With Or Without Macular Staphyloma
freq: 1/3 ev: PCS
syndrome OMIM 180849
Rubinstein-Taybi Syndrome
onset: HP:0003621 ev: PCS
syndrome OMIM 180849
Rubinstein-Taybi Syndrome 1
onset: HP:0003621 ev: PCS
syndrome OMIM 616541
Short Stature, Microcephaly, And Endocrine Dysfunction
freq: HP:0040283 ev: TAS
syndrome OMIM 182290
Smith-Magenis Syndrome
freq: 2/2 ev: PCS
syndrome OMIM 616222
Temple Syndrome
ev: TAS