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3 OMIM references -
4 associated genes
35 signs/symptoms

PROTEIN INTERACTIONS: 1

Complete androgen insensitivity syndrome

2 OMIM references -
1 associated gene
14 signs/symptoms

COFS syndrome

Complete androgen insensitivity syndrome

ERCC1	(UniProt - OMIM)		AR	(UniProt - OMIM)
ERCC2	(UniProt - OMIM)
ERCC5	(UniProt - OMIM)
ERCC6	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ERCC2	(0.56)	AR

Citations in the biomedical literature:

COFS syndrome		Complete androgen insensitivity syndrome
	Synonym(s): - Cerebrooculofacioskeletal syndrome - Pena-Shokeir syndrome type 2		Synonym(s): - CAIS - Complete androgen resistance syndrome

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic disease - Rare neurologic disease - Rare oncologic disease - Rare otorhinolaryngologic disease - Rare skin disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare endocrine disease - Rare genetic disease - Rare gynecologic or obstetric disease - Rare infertility - Rare urogenital disease

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

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

	External references: 3 OMIM references - No MeSH references		External references: 2 OMIM references - No MeSH references

COFS syndrome		Complete androgen insensitivity syndrome
	Very frequent - Anophthalmos / anophthalmia / microphthalmos / microphthalmia - Arthrogryposis - Autosomal recessive inheritance - Broad nasal root - Camptodactyly of fingers - Cataract / lens opacification - Cerebellum / cerebellar vermis anomaly / agenesis / hypoplasia - Cortical atrophy without hydrocephaly / cerebral hemiatrophy / subcortical atrophy - Death in infancy - Failure to thrive / difficulties for feeding in infancy / growth delay - Hypertonia / spasticity / rigidity / stiffness - Hypotonia - Intellectual deficit / mental / psychomotor retardation / learning disability - Intracranial / cerebral calcifications - Long / large / bulbous nose - Microcephaly - Micrognathia / retrognathia / micrognathism / retrognathism - Prominent metopic suture - Protruding lips - Restricted joint mobility / joint stiffness / ankylosis - Short stature / dwarfism / nanism - Thin / retracted lips Frequent - Areflexia / hyporeflexia - Central deafness / hearing loss - Immunodeficiency / increased susceptibility to infections / recurrent infections - Intrauterine growth retardation - Late puberty / hypogonadism / hypogenitalism - Seizures / epilepsy / absences / spasms / status epilepticus - Short neck - Skin photosensitivity - Visual loss / blindness / amblyopia Occasional - Optic nerve anomaly / optic atrophy / anomaly of the papilla - Peripheral neuropathy - Retinitis pigmentosa / retinal pigmentary changes - Talipes-varus / metatarsal varus		Very frequent - Decreased body hair / axillar / pubic hairlessness - Male pseudohermaphrodism / lack of virilisation - Primary amenorrhea - Sterility / hypofertility - Tall stature / gigantism / growth acceleration - Undescended / ectopic testes / cryptorchidia / unfixed testes - Uterine / uterus / Fallopian tubes anomalies Frequent - Inguinal / inguinoscrotal / crural hernia - Osteoporosis / osteopenia / demineralisation / osteomalacia / rickets Occasional - Contractures / cramps / trismus / tetania / claudication / opisthotonos - Gynecomastia / breast / mammary gland enlargement / hyperplasia - Sensitive trouble / deficit - Testicular / seminal neoplasm / tumor / carcinoma / cancer (excl. teratoma / germinoma) - Tremor