ODCs

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Autosomal dominant Larsen syndrome

1 OMIM reference -
1 associated gene
27 signs/symptoms

PROTEIN INTERACTIONS: 1
COMMON SIGNS: 2

Neuralgic amyotrophy

1 OMIM reference -
1 associated gene
15 signs/symptoms

Autosomal dominant Larsen syndrome

Neuralgic amyotrophy

FLNB

(UniProt - OMIM)

SEPT9

(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FLNB	(0.49)	SEPT9

Citations in the biomedical literature:

Autosomal dominant Larsen syndrome		Neuralgic amyotrophy
	Synonym(s): (no synonyms)		Synonym(s): - Acute brachial plexus neuritis - Brachial plexus neuritis - Immune brachial plexus neuropathy - Mononeuritis multiplex with brachial predilection - Neuralgic shoulder amyotrophy - Serum neuritis - Winged scapula

	Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease - Rare maxillo-facial surgical disease - Rare otorhinolaryngologic disease		Classification (Orphanet): - 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 / 1 000 000 Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: 6-9 / 10 000 Average age onset: adulthood Average age of death: normal Type of inheritance: autosomal dominant

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


COMMON SIGNS	- Respiratory distress / dyspnea / respiratory failure / lung volume reduction - Short stature / dwarfism / nanism

Autosomal dominant Larsen syndrome		Neuralgic amyotrophy
	Very frequent - Absent / small fingernails / anonychia of hands - Autosomal dominant inheritance - Autosomal recessive inheritance - Broad / bifid thumb - Depressed nasal bridge - Depressed premaxillary region / midface - Flat face - Frontal bossing / prominent forehead - Hyperextensible joints / articular hyperlaxity - Hypertelorism - Joint dislocation / subluxation - Long hand / arachnodactyly - Short hand / brachydactyly Frequent - Wrist / carpal anomalies Occasional - Cleft palate without cleft lip / submucosal cleft palate / bifid uvula - Conductive deafness / hearing loss - Craniostenosis / craniosynostosis / sutural synostosis - Epiphyseal anomaly - Intellectual deficit / mental / psychomotor retardation / learning disability - Laryngomalacia - Scoliosis - Structural anomalies of the cardio-circulatory system - Syndactyly of fingers / interdigital palm - Undescended / ectopic testes / cryptorchidia / unfixed testes - Vertebral segmentation anomaly / hemivertebrae		Very frequent - Abnormal EMG / electromyogram / electropmyography - Articular / joint pain / arthralgia - Muscle weakness / flaccidity - Neuritis / polyneuritis / multineuritis Frequent - Paresthesia / dysesthesia / hypoesthesia / anesthesia / numbness - Scapula structural / position anomaly / congenital elevation / Sprengel anomaly Occasional - Acrocyanosis / Raynaud's phenomenon / vasomotor disorders - Cleft lip and palate - Elocution disorders / dysarthria / dysphonia - Microstomia / little mouth - Peripheral neuropathy - Round face - Sleep and vigilance disorders