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Craniometaphyseal dysplasia

2 OMIM references -
2 associated genes
14 signs/symptoms

PROTEIN INTERACTIONS: 2

Spinocerebellar ataxia type 26

1 OMIM reference -
2 associated genes
No signs/symptoms info

Craniometaphyseal dysplasia

Spinocerebellar ataxia type 26

ANKH	(UniProt - OMIM)		EEF2	(UniProt - OMIM)
GJA1	(UniProt - OMIM)		SCA26	()


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	GJA1 GJA1	(0.63) (0.63)	EEF2 SCA26

Citations in the biomedical literature:

Craniometaphyseal dysplasia		Spinocerebellar ataxia type 26
	Synonym(s): - CMD		Synonym(s): - SCA26

	Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic 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: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: 2 OMIM references - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C537203

Craniometaphyseal dysplasia
	Very frequent - Autosomal dominant inheritance - Broad nasal root - Dense / thickened skull / calvarium / cranial / facial hyperostosis - Depressed nasal bridge - Hypertelorism - Metaphyseal anomaly - Osteosclerosis / osteopetrosis / bone condensation Frequent - Dysostosis / chondrodysplasia / osteodysplasia / osteochondrosis / skeletal dysplasia - Telecanthus / canthal dystopy Occasional - Conductive deafness / hearing loss - Cranial nerve anomalies - Facial palsy - Sensorineural deafness / hearing loss - Visual loss / blindness / amblyopia
Spinocerebellar ataxia type 26
(no data available)