ODCs

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Intellectual deficit, X-linked - psychosis - macroorchidism

1 OMIM reference -
1 associated gene
13 signs/symptoms

PROTEIN INTERACTIONS: 1
COMMON SIGNS: 4

Adams-Oliver syndrome

4 OMIM references -
4 associated genes
47 signs/symptoms

Intellectual deficit, X-linked - psychosis - macroorchidism

Adams-Oliver syndrome

MECP2	(UniProt - OMIM)	ARHGAP31	(UniProt - OMIM)
		DOCK6	(UniProt - OMIM)
		EOGT	(UniProt - OMIM)
		RBPJ	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MECP2	(0.72)	RBPJ

Citations in the biomedical literature:

Intellectual deficit, X-linked - psychosis - macroorchidism		Adams-Oliver syndrome
	Synonym(s): - Lindsay-Burn syndrome - PPM-X		Synonym(s): - AOS - Congenital scalp defects with distal limb anomalies - Congenital scalp defects with distal limb reduction anomalies - Limb, scalp and skull defects

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

	Classification (ICD10): - Mental and behavioural disorders -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

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

	External references: 1 OMIM reference - No MeSH references		External references: 4 OMIM references - 1 MeSH reference: C538225


COMMON SIGNS	- EEG anomalies - Hypertonia / spasticity / rigidity / stiffness - Intellectual deficit / mental / psychomotor retardation / learning disability - Seizures / epilepsy / absences / spasms / status epilepticus

Intellectual deficit, X-linked - psychosis - macroorchidism		Adams-Oliver syndrome
	Very frequent - Macroorchidism / macrotestes - Movement disorder - Psychic / behavioural troubles - X-linked recessive inheritance Frequent - Abnormal gait - Long / large ear Occasional - Psychic / psychomotor regression / dementia / intellectual decline - Scoliosis - Structural anomalies of the cardio-circulatory system		Very frequent - Autosomal dominant inheritance - Cutis marmorata / marbled skin / livedo - Failure to thrive / difficulties for feeding in infancy / growth delay - Foot absent / apodia / adactyly / acheiropodia - Global upper and lower limbs anomalies - Hand agenesis / absence - Hypotrichosis / atrichia / atrichiasis / scalp hairlessness - Lower limb segmental anomalies - Scalp / skull defect - Skin hypoplasia / aplasia / atrophy - Upper limb segmental anomalies Frequent - Anophthalmos / anophthalmia / microphthalmos / microphthalmia - Cataract / lens opacification - Hydrocephaly - Irregular length / shape of fingers - Metacarpal anomalies / Archibald's sign - Pulmonary artery stenosis / absence / hypoplasia of the pulmonary branches - Pulmonary valve atresia / stenosis / narrowing - Short hand / brachydactyly - Strabismus / squint - Syndactyly of fingers / interdigital palm - Talipes-varus / metatarsal varus - Terminal / third phalangeal bone of fingers hypoplasia - Tetralogy of Fallot / trilogy of Fallot - Trident hand / split hand / abnormal median ray Occasional - Absent / small fingernails / anonychia of hands - Absent / small toenails / anonychia of feet - Alopecia - Ascitis - Autosomal recessive inheritance - Cirrhosis - Congenital hepatic fibrosis - Encephalocele / exencephaly - Esophageal varices - Gastrointestinal bleeding / hemorrhage / hematemesis / melena / rectorrhagia - Hemiplegia / diplegia / hemiparesia / limb palsy - Leukopenia / hypoleukocytosis - Porencephaly - Portal hypertension - Prematurity - Pulmonary hypertension - Thrombocytopenia / thrombopenia - Venous stenosis