ODCs

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1 OMIM reference -
1 associated gene
12 signs/symptoms

PROTEIN INTERACTIONS: 1
COMMON SIGNS: 1

1 OMIM reference -
1 associated gene
19 signs/symptoms

Griscelli disease type 1

Spondylometaphyseal dysplasia - cone-rod dystrophy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MYO5A	(0.63)	PCYT1A

Citations in the biomedical literature:

Griscelli disease type 1		Spondylometaphyseal dysplasia - cone-rod dystrophy
	Synonym(s): - Griscelli-PruniÃ©ras syndrome type 1 - Hypopigmentation - neurologic impairment		Synonym(s): - SMD-CRD

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

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

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: no data available Average age of death: no data available Type of inheritance: autosomal recessive

	External references: 1 OMIM reference - 1 MeSH reference: C537301		External references: 1 OMIM reference - No MeSH references

Griscelli disease type 1		Spondylometaphyseal dysplasia - cone-rod dystrophy
	Very frequent - Albinism (hair) - Ataxia / incoordination / trouble of the equilibrium - Diffuse / generalised skin hypopigmentation / cutaneous albinism - Hypertonia / spasticity / rigidity / stiffness - Iris albinism / ocular albinism - Movement disorder - Premature greying of hair - Seizures / epilepsy / absences / spasms / status epilepticus Frequent - Hyperlipidemia / hypercholesterolemia / hypertriglyceridemia - Intellectual deficit / mental / psychomotor retardation / learning disability Occasional - Intracranial / cerebral calcifications		Very frequent - Bowed diaphysis / diaphyses / long bones - Hip dislocation / dysplasia / coxa valga / coxa vara / coxa plana - Metaphyseal anomaly - Platyspondyly - Retinitis pigmentosa / retinal pigmentary changes - Rhizomelic micromelia - Short stature / dwarfism / nanism Frequent - Achromatopsia / dyschromatopsia / daltonism / impaired colour vision - Astigmatism - Hypermetropia - Lordosis - Myopia - Photophobia - Rib structure anomalies - Scoliosis - Visual loss / blindness / amblyopia Occasional - Restricted joint mobility / joint stiffness / ankylosis - Short hand / brachydactyly