Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Abnormal dermatoglyphics
Very frequent (80-99%)HP:0007477
Accessory nipples
Very frequent (80-99%)HP:0002558
Capuchin ears
Very frequent (80-99%)HP:0000378
Decreased projection of lower jaw
Very frequent (80-99%)HP:0000347
Down-slanting palpebral fissure
Very frequent (80-99%)HP:0000494
Everted lower eyelids
Very frequent (80-99%)HP:0007651
Eyelid coloboma
Very frequent (80-99%)HP:0000625
Microtia
Very frequent (80-99%)HP:0008551
Posteriorly angulated ears
Very frequent (80-99%)HP:0000358
Radial ray hypoplasia
Very frequent (80-99%)HP:0002984
Short ulna
Very frequent (80-99%)HP:0003022
Zygomatic flattening
Very frequent (80-99%)HP:0000272
Abnormality of cardiovascular system morphology
Frequent (30-79%)HP:0030680
Abnormality of the middle ear
Frequent (30-79%)HP:0000370
Cleft of palate
Frequent (30-79%)HP:0000175
Hearing loss, conductive
Frequent (30-79%)HP:0000405
Non-midline cleft of the upper lip
Frequent (30-79%)HP:0100335
Partial syndactyly
Frequent (30-79%)HP:0006101
Proximal interphalangeal finger joint contractures
Frequent (30-79%)HP:0100490
Squint
Occasional (5-29%)HP:0000486
Abnormality of the feet
HP:0001760
Choanal atresia
HP:0000453
Cleft of upper lip
HP:0000204
Congenital hip dislocations
HP:0001374
Cryptorchidism
HP:0000028
Everted eyelid
HP:0000656
Fused forearm bones
HP:0002974
Growth delay as children
HP:0008897
Infantile hypertrophic pyloric stenosis
HP:0002021
Low-set ears
HP:0000369
Quick Facts
- SNOMED CT
- 66038001
- UMLS CUI
- C0265257
- Fully Specified Name
- Miller syndrome (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.