Overview
Flat forehead 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.
Baller-Gerold syndrome
Saethre-Chotzen syndrome
Autosomal dominant osteosclerosis
Spinocerebellar ataxia type 29
Always present (100%)
Component of oligomeric golgi complex 7 congenital disorder of glycosylation
Ehlers-Danlos syndrome musculocontractural type
Ehlers-Danlos syndrome progeroid type
Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome
Occasional (5-29%)
Temple Baraitser syndrome
Occasional (5-29%)
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16
Ring chromosome 7
Very frequent (80-99%)
Roifman Chitayat syndrome
Occasional (5-29%)
Kreiborg Pakistani syndrome
Frequent (30-79%)
SSM (seizures, scoliosis, macrocephaly) syndrome
Occasional (5-29%)
CAGSSS - cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome
Quick Facts
- SNOMED CT
- 1144313000
- UMLS CUI
- C1857485
- Fully Specified Name
- Flat forehead (finding)
- Associated Conditions
- 15
- 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.