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13 OMIM references -
14 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
2 associated genes
37 signs/symptoms
Autosomal dominant nonsyndromic intellectual deficit
Weaver syndrome

CACNG2 EZH2
CDH15 NSD1
CTNNB1
DOCK8
DYNC1H1
DYRK1A
EPB41L1
GRIN1
GRIN2B
KIF1A
KIRREL3
MBD5
SYNGAP1
TCF4


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CTNNB1
(0.78)
EZH2



Citations in the biomedical literature:


Autosomal dominant nonsyndromic intellectual deficit
CACNG2 CDH15 CTNNB1 DOCK8 DYNC1H1 DYRK1A
EPB41L1 GRIN1 GRIN2B KIF1A KIRREL3 MBD5
SYNGAP1 TCF4
Weaver syndrome
EZH2 NSD1



Autosomal dominant nonsyndromic intellectual deficit
Weaver syndrome

Synonym(s):
(no synonyms)

Synonym(s):
- Camptodactyly - overgrowth - unusual facies

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

Classification (ICD10):
(no data available)
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

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

External references:
13 OMIM references -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: C536687

Weaver syndrome

Very frequent
- Abnormal cry / voice / phonation disorder / nasal speech
- Advanced bone age
- Broad forehead
- Hypertelorism
- Hypertonia / spasticity / rigidity / stiffness
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Long philtrum
- Long / large ear
- Loose skin / skin relaxation / excess skin / creases
- Low set ears / posteriorly rotated ears
- Macrocephaly / macrocrania / megalocephaly / megacephaly
- Metaphyseal anomaly
- Micrognathia / retrognathia / micrognathism / retrognathism
- Tall stature / gigantism / growth acceleration
- Thin / hypoplastic toenails
- Thin / hypoplastic / hyperconvex fingernails

Frequent
- Broad foot
- Broad / bifid thumb
- Camptodactyly of fingers
- Failure to thrive / difficulties for feeding in infancy / growth delay
- Fine hair
- Inguinal / inguinoscrotal / crural hernia
- Large hand
- Philtrum deeply grooved
- Restricted joint mobility / joint stiffness / ankylosis
- Round face

Occasional
- Autosomal dominant inheritance
- Congenital cardiac anomaly / malformation / cardiopathy
- Downslanted palpebral fissures / anti-mongoloid slanting palpebral fissures
- Hyperextensible joints / articular hyperlaxity
- Micropenis / small penis / agenesis
- Pes cavus
- Scoliosis
- Syndactyly of fingers / interdigital palm
- Talipes-varus / metatarsal varus
- Undescended / ectopic testes / cryptorchidia / unfixed testes
- Wide space between 1st-2nd toes


Autosomal dominant nonsyndromic intellectual deficit

(no data available)