ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
9 signs/symptoms

Noonan syndrome-like disorder with juvenile myelomonocytic leukemia

Hereditary sensory and autonomic neuropathy type 4


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CBL	(0.72)	NTRK1

Citations in the biomedical literature:

Noonan syndrome-like disorder with juvenile myelomonocytic leukemia		Hereditary sensory and autonomic neuropathy type 4
	Synonym(s): - CBL syndrome - Noonan syndrome-like disorder with JMML		Synonym(s): - HSAN4 - Insensitivity to pain - anhidrosis - NHSA4

	Classification (Orphanet): - Rare cardiac disease - Rare developmental defect during embryogenesis - Rare genetic disease - Rare oncologic 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: (no data available)		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive

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

Hereditary sensory and autonomic neuropathy type 4
	Very frequent - Autosomal recessive inheritance - Chronic skin infection / ulcerations / ulcers / cancrum - Insensitivity to pain - Intellectual deficit / mental / psychomotor retardation / learning disability - Osteosclerosis / osteopetrosis / bone condensation - Psychic / behavioural troubles Occasional - Dental staining anomaly / spotted teeth / erythrodontia - Thick skin / pachydermia / orange skin - Tight skin / lack of elasticity
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
(no data available)