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Neurofibromatosis type 3

3 OMIM references -
3 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Brachydactyly type C

1 OMIM reference -
2 associated genes
11 signs/symptoms

Neurofibromatosis type 3

Brachydactyly type C

LZTR1	(UniProt - OMIM)		BMPR1B	(UniProt - OMIM)
NF2	(UniProt - OMIM)		GDF5	(UniProt - OMIM)
SMARCB1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	LZTR1	(0.59)	BMPR1B

Citations in the biomedical literature:

Neurofibromatosis type 3		Brachydactyly type C
	Synonym(s): - NF3 - Neurilemmomatosis - Schwannomatosis		Synonym(s): (no synonyms)

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

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant

	External references: 3 OMIM references - 1 MeSH reference: C536641		External references: 1 OMIM reference - 1 MeSH reference: C537093

Brachydactyly type C
	Very frequent - Autosomal dominant inheritance - Metacarpal anomalies / Archibald's sign - Short hand / brachydactyly - Ulnar deviation of fingers Frequent - Cone epiphyses / epiphysis - Short foot / brachydactyly of toes - Thin / hypoplastic / hyperconvex fingernails Occasional - Clinodactyly of fifth finger - Short stature / dwarfism / nanism - Symphalangy of fingers - Talipes-valgus
Neurofibromatosis type 3
(no data available)