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3 OMIM references -
3 associated genes
25 signs/symptoms
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
29 signs/symptoms
Isolated Klippel-Feil syndrome
Fragile X-associated tremor/ataxia syndrome

GDF3 FMR1
GDF6
MEOX1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
MEOX1
(0.63)
FMR1



Citations in the biomedical literature:


Isolated Klippel-Feil syndrome
GDF3 GDF6 MEOX1
Fragile X-associated tremor/ataxia syndrome
FMR1



Isolated Klippel-Feil syndrome
Fragile X-associated tremor/ataxia syndrome

Synonym(s):
- Congenital cervical vertebral fusion
- Congenital fused cervical segments
- Klippel-Feil malformation
- Klippel-Feil sequence

Synonym(s):
- FXTAS syndrome

Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: adulthood
Average age of death: elderly
Type of inheritance: x-linked dominant

External references:
3 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references

Isolated Klippel-Feil syndrome
Fragile X-associated tremor/ataxia syndrome

Very frequent
- Anomalies of spine, vertebrae and pelvis
- Autosomal dominant inheritance
- Autosomal recessive inheritance
- Facial structural asymmetry / facial hemiatrophy / facial hemihypertrophy
- Low hair line (back)
- Short neck
- Vertebral segmentation anomaly / hemivertebrae
- Webbed neck / pterygium colli

Frequent
- Anomalies of the ribs
- Congenital torticolli
- Hearing loss / hypoacusia / deafness
- Narrow / sloping shoulders
- Scapula structural / position anomaly / congenital elevation / Sprengel anomaly
- Scoliosis

Occasional
- Agenesis / hypoplasia / aplasia of kidneys
- Anus ectopia / anteposition / malposition
- Cleft palate without cleft lip / submucosal cleft palate / bifid uvula
- Congenital cardiac anomaly / malformation / cardiopathy
- Cranial nerve anomalies
- Hemiplegia / diplegia / hemiparesia / limb palsy
- Imperforate anus / rectum atresia / agenesis / recto-vaginal / vesical / perineal fistula
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Sacro-coccyx / sacrum anomaly
- Spina bifida
- Ventricular septal defect / interventricular communication


Very frequent
- Abnormal gait
- Ataxia / incoordination / trouble of the equilibrium
- Cortical atrophy without hydrocephaly / cerebral hemiatrophy / subcortical atrophy
- Elocution disorders / dysarthria / dysphonia
- Execution movement disorder / dysmetria / bradykinesia / akinesia / apraxia
- Fragile chromosome X site
- Psychic / psychomotor regression / dementia / intellectual decline
- Tremor
- Troubles of memory / amnesia / hypermnesia
- X-linked dominant inheritance

Frequent
- Areflexia / hyporeflexia
- Cerebellum / cerebellar vermis anomaly / agenesis / hypoplasia
- Dysautonomia / autonomous nervous sytem anomalies
- Humour troubles / anxiety / depression / apathy / euphoria / irritability
- Hypertonia / spasticity / rigidity / stiffness
- Impotence / painful erection / priapism / erection troubles
- Muscle weakness / flaccidity
- Obsessive-compulsive disorder
- Paresthesia / dysesthesia / hypoesthesia / anesthesia / numbness
- Peripheral neuropathy
- Pollakiuria / polyuria / dysuria / anuria / acute urine retention / oliguria
- Sphincter dysfunction

Occasional
- Chronic arterial hypertension
- Encopresis / fecal incontinence
- Feeding disorder / dysphagia / swallowing / sucking disorder / esophageal dyskinesia
- Hypotension
- Hypothyroidy
- Midbrain / brainstem / pons / medulla anomalies
- Myalgia / muscular pain