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Disease Profile
Oto-palato-digital syndrome type 1
Prevalence estimates on Rare Medical Network websites are calculated based on data available from numerous sources, including US and European government statistics, the NIH, Orphanet, and published epidemiologic studies. Rare disease population data is recognized to be highly variable, and based on a wide variety of source data and methodologies, so the prevalence data on this site should be assumed to be estimated and cannot be considered to be absolutely correct.
0
Age of onset
-
ICD-10
Q87.0
Inheritance
Autosomal dominant A pathogenic variant in only one gene copy in each cell is sufficient to cause an autosomal dominant disease.
Autosomal recessive Pathogenic variants in both copies of each gene of the chromosome are needed to cause an autosomal recessive disease and observe the mutant phenotype.
X-linked
dominant X-linked dominant inheritance, sometimes referred to as X-linked dominance, is a mode of genetic inheritance by which a dominant gene is carried on the X chromosome.
dominant X-linked dominant inheritance, sometimes referred to as X-linked dominance, is a mode of genetic inheritance by which a dominant gene is carried on the X chromosome.
X-linked
recessive Pathogenic variants in both copies of a gene on the X chromosome cause an X-linked recessive disorder.
recessive Pathogenic variants in both copies of a gene on the X chromosome cause an X-linked recessive disorder.
Mitochondrial or multigenic Mitochondrial genetic disorders can be caused by changes (mutations) in either the mitochondrial DNA or nuclear DNA that lead to dysfunction of the mitochondria and inadequate production of energy.
Multigenic or multifactor Inheritance involving many factors, of which at least one is genetic but none is of overwhelming importance, as in the causation of a disease by multiple genetic and environmental factors.
Not applicable
Other names (AKA)
Otopalatodigital syndrome type 1; Taybi syndrome; OPD syndrome;
Categories
Congenital and Genetic Diseases; Ear, Nose, and Throat Diseases; Mouth Diseases;
Summary
Orpha Number: 90650
Symptoms
This table lists symptoms that people with this disease may have. For most diseases, symptoms will vary from person to person. People with the same disease may not have all the symptoms listed. This information comes from a database called the Human Phenotype Ontology (HPO) . The HPO collects information on symptoms that have been described in medical resources. The HPO is updated regularly. Use the HPO ID to access more in-depth information about a symptom.
Medical Terms | Other Names |
Learn More:
HPO ID
|
---|---|---|
80%-99% of people have these symptoms | ||
Anodontia |
Failure of development of all teeth
|
0000674 |
Cleft roof of mouth
|
0000175 | |
Depressed nasal bridge |
Depressed bridge of nose
Flat bridge of nose
Flat nasal bridge
Flat, nasal bridge
Flattened nasal bridge
Low nasal bridge
Low nasal root
[ more ] |
0005280 |
Downslanted palpebral fissures |
Downward slanting of the opening between the eyelids
|
0000494 |
Hearing impairment |
Deafness
Hearing defect
[ more ] |
0000365 |
Hypertelorism |
Wide-set eyes
Widely spaced eyes
[ more ] |
0000316 |
Mental retardation, borderline-mild
Mild and nonprogressive mental retardation
Mild mental retardation
[ more ] |
0001256 | |
Limitation of joint mobility |
Decreased joint mobility
Decreased mobility of joints
Limited joint mobility
Limited joint motion
[ more ] |
0001376 |
Oligodontia |
Failure of development of more than six teeth
|
0000677 |
Prominent supraorbital ridges |
Prominent brow
|
0000336 |
Sandal gap |
Gap between 1st and 2nd toes
Gap between first and second toe
Increased space between first and second toes
Sandal gap between first and second toes
Wide space between 1st, 2nd toes
Wide space between first and second toes
Wide-spaced big toe
Widely spaced 1st-2nd toes
Widely spaced first and second toes
Widened gap 1st-2nd toes
Widened gap first and second toe
[ more ] |
0001852 |
Short hallux |
Short big toe
|
0010109 |
Skeletal dysplasia | 0002652 | |
Wide nasal bridge |
Broad nasal bridge
Broad nasal root
Broadened nasal bridge
Increased breadth of bridge of nose
Increased breadth of nasal bridge
Increased width of bridge of nose
Increased width of nasal bridge
Nasal bridge broad
Wide bridge of nose
Widened nasal bridge
[ more ] |
0000431 |
30%-79% of people have these symptoms | ||
Abnormality of the metacarpal bones |
Abnormality of the long bone of hand
|
0001163 |
Bowing of the long bones |
Bowed long bones
Bowing of long bones
[ more ] |
0006487 |
Elbow dislocation |
Dislocations of the elbows
Elbow dislocations
[ more ] |
0003042 |
Hypoplastic frontal sinuses | 0002738 | |
Increased bone mineral density |
Increased bone density
|
0011001 |
Proximal placement of thumb |
Attachment of thumb close to wrist
|
0009623 |
Short distal phalanx of finger |
Short outermost finger bone
|
0009882 |
Short palm | 0004279 | |
Short thumb |
Short thumbs
Small thumbs
[ more ] |
0009778 |
Thickened calvaria |
Increased thickness of skull cap
Thickened skull cap
[ more ] |
0002684 |
5%-29% of people have these symptoms | ||
Abnormal vertebral segmentation and fusion | 0005640 | |
Abnormality of the tarsal bones |
Abnormal ankle bones
|
0001850 |
Synostosis of carpal bones |
Fusion of wrist bones
|
0005048 |
Percent of people who have these symptoms is not available through HPO | ||
Abnormality of the fifth metatarsal bone |
Abnormality of the 5th long bone of foot
|
0008089 |
Absent frontal sinuses | 0002688 | |
Accessory carpal bones | 0004232 | |
Bipartite calcaneus | 0008127 | |
Broad distal phalanx of the thumb |
Broad outermost bone of the thumb
Wide outermost bone of thumb
[ more ] |
0009642 |
Broad hallux |
Broad big toe
Wide big toe
[ more ] |
0010055 |
Bulbous tips of toes | 0001782 | |
Capitate-hamate fusion | 0001241 | |
Conductive hearing impairment |
Conductive deafness
Conductive hearing loss
[ more ] |
0000405 |
Coxa valga | 0002673 | |
Delayed closure of the anterior fontanelle |
Later than typical closing of soft spot of skull
|
0001476 |
Dislocated radial head | 0003083 | |
Flat face |
Flat facial shape
|
0012368 |
Frontal bossing | 0002007 | |
Hip dislocation |
Dislocated hips
Dislocation of hip
[ more ] |
0002827 |
Lateral femoral bowing | 0005090 | |
Limited elbow extension |
Decreased elbow extension
Elbow limited extension
Limitation of elbow extension
Limited extension at elbows
Limited forearm extension
Restricted elbow extension
[ more ] |
0001377 |
Limited knee flexion | 0006389 | |
Malar flattening |
Zygomatic flattening
|
0000272 |
Multiple impacted teeth |
Impacted teeth
|
0001571 |
Nail dysplasia |
Atypical nail growth
|
0002164 |
Nail dystrophy |
Poor nail formation
|
0008404 |
Narrow mouth |
Small mouth
|
0000160 |
Omphalocele | 0001539 | |
Pectus excavatum |
Funnel chest
|
0000767 |
Prominent occiput |
Prominent back of the skull
Prominent posterior skull
[ more ] |
0000269 |
0002650 | ||
Selective tooth agenesis | 0001592 | |
Short 3rd metacarpal |
Shortened 3rd long bone of hand
|
0010041 |
Short 4th metacarpal |
Shortened 4th long bone of hand
|
0010044 |
Short 5th metacarpal |
Shortened 5th long bone of hand
|
0010047 |
Short nose
DiagnosisMaking a diagnosis for a genetic or rare disease can often be challenging. Healthcare professionals typically look at a person’s medical history, symptoms, physical exam, and laboratory test results in order to make a diagnosis. The following resources provide information relating to diagnosis and testing for this condition. If you have questions about getting a diagnosis, you should contact a healthcare professional. Testing Resources
Learn moreThese resources provide more information about this condition or associated symptoms. The in-depth resources contain medical and scientific language that may be hard to understand. You may want to review these resources with a medical professional. In-Depth Information
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