ODCs

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
16 signs/symptoms

Noonan syndrome-like disorder with juvenile myelomonocytic leukemia

Fetal Gaucher disease


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CBL	(0.63)	GBA

Citations in the biomedical literature:

Noonan syndrome-like disorder with juvenile myelomonocytic leukemia		Fetal Gaucher disease
	Synonym(s): - CBL syndrome - Noonan syndrome-like disorder with JMML		Synonym(s): - Perinatal lethal Gaucher disease

	Classification (Orphanet): - Rare cardiac disease - Rare developmental defect during embryogenesis - Rare genetic disease - Rare oncologic disease		Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare skin disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: (no data available)		Epidemiological data: (no data available)

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

Fetal Gaucher disease
	Very frequent - Death in infancy - Hydrops fetalis - Ichthyosis / ichthyosiform dermatitis - Intracranial / cerebral / meningeal hemorrhage - Stillbirth / neonatal death - Thrombocytopenia / thrombopenia Frequent - Depressed nasal bridge - Ectropion / entropion / eyelid eversion - Hepatomegaly / liver enlargement (excluding storage disease) - High vaulted / narrow palate - Hypertonia / spasticity / rigidity / stiffness - Hypotonia - Low set ears / posteriorly rotated ears - Seizures / epilepsy / absences / spasms / status epilepticus - Splenomegaly - Structural and functional anomalies of the spleen
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
(no data available)