Overview
Thin build is a finding that may indicate an underlying health condition requiring clinical evaluation.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Marfan's syndrome
Very frequent (80-99%)
Diaphyseal dysplasia
Occasional (5-29%)
Werner syndrome
Very frequent (80-99%)
Stickler syndrome
Occasional (5-29%)
CCA - Congenital contractural arachnodactyly
Very frequent (80-99%)
Neonatal pseudo-hydrocephalic progeroid syndrome
Very frequent (80-99%)
Multiple symmetrical lipomatosis
Very frequent (80-99%)
Deletion of long arm of chromosome 18
Occasional (5-29%)
Nemaline myopathy 3
Mitochondrial neurogastrointestinal encephalomyopathy syndrome
Brain calcification Rajab type
Lipodystrophy, intellectual disability, deafness syndrome
Very frequent (80-99%)
Thoracolaryngopelvic dysplasia
Sillence syndrome
Occasional (5-29%)
CK syndrome
Very frequent (80-99%)
Mitochondrial DNA deletion syndrome with limb-girdle weakness
Frequent (30-79%)
Distal nebulin myopathy
Occasional (5-29%)
X-linked intellectual disability due to GRIA3 mutations
Frequent (30-79%)
PMSE (polyhydramnios, megalencephaly, symptomatic epilepsy) syndrome
Macrocephaly, intellectual disability, left ventricular non compaction syndrome
Frequent (30-79%)
Childhood-onset nemaline myopathy
Occasional (5-29%)
3-methylglutaconic aciduria, epilepsy, spasticity, severe intellectual disability syndrome
Very frequent (80-99%)
FG syndrome type 1
Frequent (30-79%)
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome
Frequent (30-79%)
Quick Facts
- SNOMED CT
- 61294007
- UMLS CUI
- C0039870
- Fully Specified Name
- Thin build (finding)
- Associated Conditions
- 24
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.