Overview
Craniolenticulosutural dysplasia is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Decreased volume of upper lip
Always present (100%)HP:0000219
Flat midface
Always present (100%)HP:0011800
Increased width of bridge of nose
Always present (100%)HP:0000431
Narrow iliac wing
Always present (100%)HP:0002868
Persistent anterior fontanelle
Always present (100%)HP:0001476
Wider-than-typical soft spot of skull
Always present (100%)HP:0000260
Abnormal skeletal development
Very frequent (80-99%)HP:0002652
Brittle hair
Very frequent (80-99%)HP:0002299
Coarse hair texture
Very frequent (80-99%)HP:0002208
Decreased body height
Very frequent (80-99%)HP:0004322
Decreased mineralization of skull
Very frequent (80-99%)HP:0004331
Decreased volume of lip vermillion
Very frequent (80-99%)HP:0000233
Decreased width of tooth
Very frequent (80-99%)HP:0000691
Delayed eruption of teeth
Very frequent (80-99%)HP:0000684
Flat philtrum
Very frequent (80-99%)HP:0000319
Frontal protuberance
Very frequent (80-99%)HP:0002007
High iliac wing
Very frequent (80-99%)HP:0008808
Hypoplastic teeth
Very frequent (80-99%)HP:0000685
Hypotrophic maxilla
Very frequent (80-99%)HP:0000327
Increased distance between eyes
Very frequent (80-99%)HP:0000316
Increased length of philtrum
Very frequent (80-99%)HP:0000343
Increased nasal width
Very frequent (80-99%)HP:0000445
Large fontanelle
Very frequent (80-99%)HP:0000239
Large mouth
Very frequent (80-99%)HP:0000154
Posterior wedging
Very frequent (80-99%)HP:0008444
Posterior Y-sutural cataract
Very frequent (80-99%)HP:0008031
Premature exfoliation of teeth
Very frequent (80-99%)HP:0006480
Prominent nasal root
Very frequent (80-99%)HP:0000426
Prominent supraorbital margins
Very frequent (80-99%)HP:0000336
Rotting teeth
Very frequent (80-99%)HP:0000670
Related Conditions
Orbital hypertelorism(parent)
Multiple system malformation syndrome(parent)
Recessive hereditary disorder (autosomal)(parent)
Congenital enlargement of fontanel(parent)
Skeletal dysplasia(parent)
Small stature(parent)
Hereditary disorder of musculoskeletal system(parent)
Developmental hereditary disorder(parent)
Quick Facts
- SNOMED CT
- 725100001
- UMLS CUI
- C1843042
- Fully Specified Name
- Craniolenticulosutural dysplasia (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 30
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.