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6 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
4 OMIM references -
4 associated genes
78 signs/symptoms
Semantic dementia
Cardiofaciocutaneous syndrome

C9ORF72 BRAF
CHMP2B KRAS
GRN MAP2K1
MAPT MAP2K2
PSEN1
VCP


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
VCP
(0.63)
MAP2K1



Citations in the biomedical literature:


Semantic dementia
C9ORF72 CHMP2B GRN MAPT PSEN1 VCP

Cardiofaciocutaneous syndrome
BRAF KRAS MAP2K1 MAP2K2



Semantic dementia
Cardiofaciocutaneous syndrome

Synonym(s):
- Semantic primary progressive aphasia
- Semantic variant PPA

Synonym(s):
- CFC syndrome

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

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
Class of prevalence: -
Average age onset: adulthood
Average age of death: -
Type of inheritance: multigenic/multifactorial
Epidemiological data:
(no data available)

External references:
No OMIM references
No MeSH references
External references:
4 OMIM references -
1 MeSH reference: C535579

Cardiofaciocutaneous syndrome

Very frequent
- Absent / decreased / thin eyebrows
- Anomalies of eyelids, eyelashes and lacrimal system
- Anomalies of eyes and vision
- Anteverted nares / nostrils
- Atrial septal defect / interauricular communication
- Autosomal dominant inheritance
- Brittle hair / distrix / trichorrhexis
- Broad cheeks / cherub-like / cherubin face
- Cardiac valvulopathy
- Coarse face
- Congenital cardiac anomaly / malformation / cardiopathy
- Dry / squaly skin / exfoliation
- Euryblepharon / wide palpebral fissures
- Failure to thrive / difficulties for feeding in infancy / growth delay
- Fine hair
- Flat supraorbital ridge
- Hairy patch
- Helix thickened / sculpted
- Hypotonia
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Long face
- Palmoplantar hyperkeratosis / keratoderma
- Pulmonary artery stenosis / absence / hypoplasia of the pulmonary branches
- Rippled skin
- Short stature / dwarfism / nanism
- Speech troubles / aphasia / dysphasia / echolalia / mutism / logorrhea / dysprosodia

Frequent
- Absent / decreased lashes
- Cafe-au-lait spot
- Capillary hemangioma / nevus / naevus flammeus / port-wine stain
- Deep palmar creases
- Depressed nasal bridge
- Diffuse / generalised skin hyperpigmentation / melanoderma
- Downslanted palpebral fissures / anti-mongoloid slanting palpebral fissures
- Dysplastic / thick / grooved fingernails
- EEG anomalies
- Epicanthic folds
- Flat cheek bones / malar hypoplasia
- Frontal bossing / prominent forehead
- High forehead
- High vaulted / narrow palate
- Hyperelastic skin / cutaneous hyperlaxity
- Hyperkeratosis / ainhum / hyperkeratotic skin fissures
- Hypertelorism
- Hypotrichosis / atrichia / atrichiasis / scalp hairlessness
- Ichthyosis / ichthyosiform dermatitis
- Long philtrum
- Long / large ear
- Low hair line (back)
- Low set ears / posteriorly rotated ears
- Macrocephaly / macrocrania / megalocephaly / megacephaly
- Myopia
- Narrow forehead
- Nystagmus
- Pectus excavatum
- Prematurity
- Ptosis
- Scoliosis
- Short neck
- Short / small nose
- slow growth of the hair
- Strabismus / squint
- Ulnar / cubital anomaly / absence / agenesis / hypoplasia / abnormal ulnar / cubital ray
- Undescended / ectopic testes / cryptorchidia / unfixed testes
- Webbed neck / pterygium colli

Occasional
- Cardiomyopathy / hypertrophic / dilated
- Cleft palate without cleft lip / submucosal cleft palate / bifid uvula
- Cortical atrophy without hydrocephaly / cerebral hemiatrophy / subcortical atrophy
- Cubitus valgus
- Elocution disorders / dysarthria / dysphonia
- Functional anomalies of the digestive system
- Genu valgum
- Hydrocephaly
- Late puberty / hypogonadism / hypogenitalism
- Loose skin / skin relaxation / excess skin / creases
- Lymphedema
- Megaureter / hydronephrosis / pyeloureteral junction syndrome
- Optic nerve anomaly / optic atrophy / anomaly of the papilla
- Structural anomalies of the digestive tract


Semantic dementia

(no data available)