ODCs

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
28 signs/symptoms

Hereditary combined deficiency of vitamin K-dependent clotting factors

X-linked dominant chondrodysplasia punctata

GGCX	(UniProt - OMIM)		EBP	(UniProt - OMIM)
VKORC1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	VKORC1	(0.72)	EBP

Citations in the biomedical literature:

Hereditary combined deficiency of vitamin K-dependent clotting factors		X-linked dominant chondrodysplasia punctata
	Synonym(s): - Hereditary combined deficiency of factors II, VII, IX and X		Synonym(s): - CDPX2 - CDPXD - CPXD - Chondrodystrophia calcificans congenita - Conradi-HÃ¼nermann-Happle syndrome - X-linked chondrodysplasia punctata type 2

	Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare hematologic disease		Classification (Orphanet): - Inborn errors of metabolism - Rare bone disease - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic disease - Rare skin disease

	Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: x-linked dominant

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

X-linked dominant chondrodysplasia punctata
	Very frequent - Decreased body hair / axillar / pubic hairlessness - Dysplastic / thick / grooved fingernails - Epicanthic folds - Erythema / erythematous lesions / erythroderma / polymorphous erythema - Ichthyosis / ichthyosiform dermatitis - Joint / articular deformation - Kyphosis - Ptosis - Short stature / dwarfism / nanism - Upper limb asymmetry / hemiatrophy / hemihypertrophy Frequent - Optic nerve anomaly / optic atrophy / anomaly of the papilla Occasional - Abnormal dentition / dental position / implantation / unerupted / dental ankylosis - Abnormal vertebral size / shape - Anophthalmos / anophthalmia / microphthalmos / microphthalmia - Brittle hair / distrix / trichorrhexis - Cataract / lens opacification - Clinodactyly of fifth finger - Epiphyseal anomaly - Flat cheek bones / malar hypoplasia - Flat face - Frontal bossing / prominent forehead - Hip dislocation / dysplasia / coxa valga / coxa vara / coxa plana - Microcornea - Polydactyly of toes - Rhizomelic micromelia - Sensorineural deafness / hearing loss - Skin hypoplasia / aplasia / atrophy - Talipes-varus / metatarsal varus
Hereditary combined deficiency of vitamin K-dependent clotting factors
(no data available)