ODCs

Cytoscape Web

Click node...

Frontometaphyseal dysplasia

1 OMIM reference -
1 associated gene
33 signs/symptoms

PROTEIN INTERACTIONS: 1
COMMON SIGNS: 1

Familial dysautonomia

1 OMIM reference -
1 associated gene
37 signs/symptoms

Frontometaphyseal dysplasia

Familial dysautonomia

(UniProt - OMIM)

(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FLNA	(0.63)	IKBKAP

Citations in the biomedical literature:

Frontometaphyseal dysplasia		Familial dysautonomia
	Synonym(s): (no synonyms)		Synonym(s): - HSAN3 - Hereditary sensory and autonomic neuropathy type 3 - Riley-Day syndrome

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

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

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: x-linked dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive

	External references: 1 OMIM reference - 1 MeSH reference: C538064		External references: 1 OMIM reference - 1 MeSH reference: D004402


COMMON SIGNS	- Scoliosis

Frontometaphyseal dysplasia		Familial dysautonomia
	Very frequent - Bowed diaphysis / diaphyses / long bones - Camptodactyly of fingers - Dense / thickened skull / calvarium / cranial / facial hyperostosis - Diaphyseal anomaly - Downslanted palpebral fissures / anti-mongoloid slanting palpebral fissures - Frontal sinus agenesis / anomaly - Hypertelorism - Metaphyseal anomaly - Micrognathia / retrognathia / micrognathism / retrognathism - Prominent supraorbital ridge - Restricted joint mobility / joint stiffness / ankylosis - Tooth shape anomaly - X-linked recessive inheritance Frequent - Abnormal vertebral size / shape - Advanced bone age - Carpal bones fusion / synostosis - Conductive deafness / hearing loss - Elbow dislocation - High vaulted / narrow palate - Long hand / arachnodactyly - Muscle hypotrophy / atrophy / dystrophy / agenesis / amyotrophy - Sensorineural deafness / hearing loss - Thumb hypoplasia / aplasia / absence - Ulnar deviation of fingers Occasional - Atrioventricular canal - Autosomal dominant inheritance - Craniostenosis / craniosynostosis / sutural synostosis - Larynx / laryngeal stenosis / atresia - Megaureter / hydronephrosis / pyeloureteral junction syndrome - Tracheal atresia / stenosis - Ureteral stenosis / narrowing - Urethral anomalies / stenosis / posterior urethral valves / megalocystis		Very frequent - Abnormal EMG / electromyogram / electropmyography - Anomalies of eyelids, eyelashes and lacrimal system - Areflexia / hyporeflexia - Autosomal recessive inheritance - Failure to thrive / difficulties for feeding in infancy / growth delay - Hyperhidrosis / increased sweating - Hypohidrosis / decreased sweating / thermoregulation disorder / heat intolerance - Hypotension - Insensitivity to pain - Malignant hyperthermia - Peripheral neuropathy - Pupillary anomalies / mydriasis / myosis / tonic pupil Frequent - Abnormal gait - Ataxia / incoordination / trouble of the equilibrium - Chronic arterial hypertension - Corneal ulceration / perforation - Hypotonia - Psychic / behavioural troubles - Repeat respiratory infections Occasional - Abnormal pleura / hydrothorax / pleuresia / pleural effusion / chylothorax - Acrocyanosis / Raynaud's phenomenon / vasomotor disorders - Cardiac rhythm disorder / arrhythmia - Corneal clouding / opacity / vascularisation - Gastroesophageal reflux / pyrosis / esophagitis / hiatal hernia / gastroparesia - Heterochromia / mixed colouring of iris - Hyponatremia - Mutiple fractures / bone fragility - Myopia - Optic nerve anomaly / optic atrophy / anomaly of the papilla - Osteolysis / osteoclasia / bone destruction / erosions - Osteonecrosis / bone infarction - Renal failure - Renal glomerular defect / glomerulopathy - Renal / kidney anomalies - Seizures / epilepsy / absences / spasms / status epilepticus - Structural anomaly of the peritoneum