Overview
Nasodigitoacoustic syndrome 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.
Increased nasal width
Always present (100%)HP:0000445
Absent/hypoplastic terminal phalanges of toes
Very frequent (80-99%)HP:0010185
Broad bone of big toe
Very frequent (80-99%)HP:0010059
Broad distal phalanx of finger
Very frequent (80-99%)HP:0009836
Broad thumbs
Very frequent (80-99%)HP:0011304
Concave bridge of nose
Very frequent (80-99%)HP:0005280
Distal phalangeal hypoplasia
Very frequent (80-99%)HP:0009882
Increased distance between eyes
Very frequent (80-99%)HP:0000316
Increased width of the forehead
Very frequent (80-99%)HP:0000337
Nonprogressive mental retardation
Very frequent (80-99%)HP:0001249
Prominent nasal root
Very frequent (80-99%)HP:0000426
Sensorineural deafness
Very frequent (80-99%)HP:0000407
Short hallux
Very frequent (80-99%)HP:0010109
Abnormality of cardiovascular system morphology
Frequent (30-79%)HP:0030680
Aplastic/hypoplastic toenails
Frequent (30-79%)HP:0010624
Brachydactyly
Frequent (30-79%)HP:0001156
Broad big toe
Frequent (30-79%)HP:0010055
Bulging forehead
Frequent (30-79%)HP:0011220
Camptodactyly
Frequent (30-79%)HP:0012385
Clinodactyly
Frequent (30-79%)HP:0030084
Cupid-bow shaped upper lip
Frequent (30-79%)HP:0002263
Curvature of little finger
Frequent (30-79%)HP:0004209
Downturned corners of mouth
Frequent (30-79%)HP:0002714
Eyelid ptosis
Frequent (30-79%)HP:0000508
Husky voice
Frequent (30-79%)HP:0001609
Large head
Frequent (30-79%)HP:0000256
Low-set ears
Frequent (30-79%)HP:0000369
Palpebronasal fold
Frequent (30-79%)HP:0000286
Small midface
Frequent (30-79%)HP:0011800
Small upper jaw
Frequent (30-79%)HP:0000327
Related Conditions
Congenital anomaly of skeletal bone(parent)
Multiple malformation syndrome with facial-limb defects as major feature(parent)
Hearing loss associated with syndrome(parent)
Hereditary disorder of musculoskeletal system(parent)
Congenital sensorineural hearing loss(parent)
Disorder of ear(parent)
Developmental hereditary disorder(parent)
Hereditary hearing loss(parent)
Abnormality of limb bone morphology(parent)
Quick Facts
- SNOMED CT
- 763774001
- UMLS CUI
- C1850627
- Fully Specified Name
- Keipert 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.