Cytoscape Web
Click node...


5 OMIM references -
5 associated genes
54 signs/symptoms
PROTEIN INTERACTIONS: 1
COMMON SIGNS: 2
1 OMIM reference -
1 associated gene
21 signs/symptoms
Coffin-Siris syndrome
Richieri Costa-Pereira syndrome

ARID1A EIF4A3
ARID1B
SMARCA4
SMARCB1
SMARCE1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
SMARCB1
(0.49)
EIF4A3



Citations in the biomedical literature:


Coffin-Siris syndrome
ARID1A ARID1B SMARCA4 SMARCB1 SMARCE1
Richieri Costa-Pereira syndrome
EIF4A3



Coffin-Siris syndrome
Richieri Costa-Pereira syndrome

Synonym(s):
- CSS

Synonym(s):
- Short stature - Pierre Robin sequence - cleft mandible - hand anomalies clubfoot
- Short stature - Pierre Robin syndrome - cleft mandible - hand anomalies clubfoot

Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare maxillo-facial surgical disease
- Rare otorhinolaryngologic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
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: child / adolescent
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 recessive

External references:
5 OMIM references -
1 MeSH reference: C536436
External references:
1 OMIM reference -
1 MeSH reference: C535677


COMMON
SIGNS
- Cleft palate without cleft lip / submucosal cleft palate / bifid uvula
- Short stature / dwarfism / nanism


Coffin-Siris syndrome
Richieri Costa-Pereira syndrome

Very frequent
- Absent / small fingernails / anonychia of hands
- Anomalies of teeth and dentition
- Broad nose / nasal bridge
- Coarse face
- Feeding disorder / dysphagia / swallowing / sucking disorder / esophageal dyskinesia
- Hirsutism / hypertrichosis / Increased body hair
- Hypotonia
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Long / thick / curved lashes / trichomegaly / polytrichia
- Microcephaly
- slow growth of the hair
- Terminal / third phalangeal bone of fingers hypoplasia
- Thick lips
- Thick / bushy eyebrows

Frequent
- Cerebellum / cerebellar vermis anomaly / agenesis / hypoplasia
- Congenital cardiac anomaly / malformation / cardiopathy
- Dandy-Walker anomaly
- Depressed nasal bridge
- Elbow dislocation
- Flattened nose
- Hearing loss / hypoacusia / deafness
- Hyperextensible joints / articular hyperlaxity
- Intrauterine growth retardation
- Macrostomia / big mouth
- Nystagmus
- Patella absent / abnormal (excluding luxation)
- Repeat respiratory infections
- Scoliosis
- Seizures / epilepsy / absences / spasms / status epilepticus
- Strabismus / squint
- Undescended / ectopic testes / cryptorchidia / unfixed testes

Occasional
- Absent / small toenails / anonychia of feet
- Agenesis / hypoplasia / aplasia of kidneys
- Anomalies of spine, vertebrae and pelvis
- Cataract / lens opacification
- Clavicle absent / abnormal
- Corpus callosum / septum pellucidum total / partial agenesis
- Cutis marmorata / marbled skin / livedo
- Defect / anomaly of lacrimal system
- Diaphragmatic hernia / defect / agenesis
- Dilated cerebral ventricles without hydrocephaly
- Ectopic / horseshoe / fused kidneys
- Epicanthic folds
- Herniae
- Hip dislocation / dysplasia / coxa valga / coxa vara / coxa plana
- Intervertebral disk anomaly
- Kyphosis
- Megaureter / hydronephrosis / pyeloureteral junction syndrome
- Ptosis
- Short philtrum
- Simian crease / transverse / unique palmar crease
- Spina bifida occulta


Very frequent
- Autosomal recessive inheritance
- Low set ears / posteriorly rotated ears
- Micrognathia / retrognathia / micrognathism / retrognathism
- Microstomia / little mouth
- Prominent / bat ears
- Radial club hand
- Talipes-varus / metatarsal varus
- Thumb hypoplasia / aplasia / absence

Frequent
- Anodontia / oligodontia / hypodontia
- Clinodactyly of fifth finger
- Facial cleft
- Failure to thrive / difficulties for feeding in infancy / growth delay
- Glossoptosis
- Metacarpal anomalies / Archibald's sign
- Radius anomaly / absence / agenesis / hypoplasia / abnormal radial ray
- Respiratory distress / dyspnea / respiratory failure / lung volume reduction

Occasional
- High vaulted / narrow palate
- Proximally set thumb
- Tibia anomaly (excluding short) / absence / agenesis / hypoplasia / tibial ray anomaly