National Center for Advancing and Translational Sciences Genetic and Rare Diseases Information Center, a program of the National Center for Advancing and Translational Sciences

Gollop Coates syndrome



Other Names:
Bifurcation of distal humerus with oligoectro-syndactyly

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.

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Medical Terms Other Names
Learn More:
HPO ID
30%-79% of people have these symptoms
Broad forehead
Increased width of the forehead
Wide forehead
[ more ]
0000337
Highly arched eyebrow
Arched eyebrows
Broad, arched eyebrows
High, rounded eyebrows
High-arched eyebrows
Thick, flared eyebrows
[ more ]
0002553
Long philtrum 0000343
Sparse and thin eyebrow
Thin, sparse eyebrows
0000535
Percent of people who have these symptoms is not available through HPO
Aortic regurgitation 0001659
Aortic valve stenosis
Narrowing of aortic valve
0001650
Arthralgia
Joint pain
0002829
Arthropathy
Disease of the joints
0003040
Autosomal dominant inheritance 0000006
Autosomal recessive inheritance 0000007
Barrel-shaped chest
Barrel chest
0001552
Bilateral single transverse palmar creases 0007598
Brachydactyly
Short fingers or toes
0001156
Camptodactyly of finger
Permanent flexion of the finger
0100490
Coronal cleft vertebrae 0003417
Cubitus valgus
Outward turned elbows
0002967
Decreased hip abduction 0003184
Delayed eruption of teeth
Delayed eruption
Delayed teeth eruption
Delayed tooth eruption
Eruption, delayed
Late eruption of teeth
Late tooth eruption
[ more ]
0000684
Delayed gross motor development
Delayed motor skills
0002194
Delayed skeletal maturation
Delayed bone maturation
Delayed skeletal development
[ more ]
0002750
Deviation of the 5th finger
Displaced little finger
Displaced pinkie finger
Displaced pinky finger
[ more ]
0009179
Elbow dislocation
Dislocations of the elbows
Elbow dislocations
[ more ]
0003042
Fixed elbow flexion 0006471
Flattened epiphysis
Flat end part of bone
0003071
Generalized bone demineralization 0006462
Genu valgum
Knock knees
0002857
Hearing impairment
Deafness
Hearing defect
[ more ]
0000365
High palate
Elevated palate
Increased palatal height
[ more ]
0000218
Hypertelorism
Wide-set eyes
Widely spaced eyes
[ more ]
0000316
Hypoplasia of the capital femoral epiphysis
Small innermost thighbone end part
Underdevelopment of the innermost thighbone end part
[ more ]
0003090
Hypoplasia of the ulna
Underdeveloped inner large forearm bone
0003022
Intervertebral space narrowing 0002945
Irregular vertebral endplates 0003301
Knee dislocation 0004976
Kyphoscoliosis 0002751
Limited hip extension
Restricted hip extension
0003093
Lumbar hyperlordosis
Excessive inward curvature of lower spine
0002938
Microdontia
Decreased width of tooth
0000691
Microtia
Small ears
Underdeveloped ears
[ more ]
0008551
Mitral regurgitation 0001653
Mitral stenosis 0001718
Multiple carpal ossification centers 0006067
Narrow vertebral interpedicular distance 0008450
Pes planus
Flat feet
Flat foot
[ more ]
0001763
Pulmonary arterial hypertension
Increased blood pressure in blood vessels of lungs
0002092
Pulmonic stenosis
Narrowing of pulmonic valve
0001642
Rhizomelia
Disproportionately short upper portion of limb
0008905
Shield chest 0000914
Short distal phalanx of finger
Short outermost finger bone
0009882
Short femoral neck
Short neck of thighbone
0100864
Short metacarpal
Shortened long bone of hand
0010049
Short neck
Decreased length of neck
0000470
Shoulder dislocation 0003834
Small epiphyses
Small end part of bone
0010585
Spondyloepiphyseal dysplasia 0002655
Talipes equinovarus
Club feet
Club foot
Clubfeet
Clubfoot
[ more ]
0001762
Tibial bowing
Bowed shankbone
Bowed shinbone
[ more ]
0002982
Tricuspid regurgitation 0005180
Tricuspid stenosis 0010446
Ulnar bowing
Curving of inner forearm bone
0003031
Ventricular hypertrophy 0001714
Ventricular septal defect
Hole in heart wall separating two lower heart chambers
0001629
Waddling gait
'Waddling' gait
Waddling walk
[ more ]
0002515
Wide intermamillary distance
Wide-spaced nipples
Widely spaced nipples
Widely-spaced nipples
[ more ]
0006610
Widely spaced teeth
Wide-spaced teeth
Widely-spaced teeth
[ more ]
0000687
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Last updated: 7/1/2020

If you need medical advice, you can look for doctors or other healthcare professionals who have experience with this disease. You may find these specialists through advocacy organizations, clinical trials, or articles published in medical journals. You may also want to contact a university or tertiary medical center in your area, because these centers tend to see more complex cases and have the latest technology and treatments.

If you can’t find a specialist in your local area, try contacting national or international specialists. They may be able to refer you to someone they know through conferences or research efforts. Some specialists may be willing to consult with you or your local doctors over the phone or by email if you can't travel to them for care.

You can find more tips in our guide, How to Find a Disease Specialist. We also encourage you to explore the rest of this page to find resources that can help you find specialists.

Healthcare Resources


These 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

  • The Monarch Initiative brings together data about this condition from humans and other species to help physicians and biomedical researchers. Monarch’s tools are designed to make it easier to compare the signs and symptoms (phenotypes) of different diseases and discover common features. This initiative is a collaboration between several academic institutions across the world and is funded by the National Institutes of Health. Visit the website to explore the biology of this condition.
  • Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine. 
  • PubMed is a searchable database of medical literature and lists journal articles that discuss Gollop Coates syndrome. Click on the link to view a sample search on this topic.

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