Cytoscape Web
Click node...


1 OMIM reference -
1 associated gene
49 signs/symptoms
PROTEIN INTERACTIONS: 1
COMMON SIGNS: 1
6 OMIM references -
10 associated genes
8 signs/symptoms
Camurati-Engelmann disease
Oligodontia

TGFB1 AXIN2
EDA
EDARADD
FGFR1
IRF6
LTBP3
MSX1
PAX9
TGFA
WNT10A


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
TGFB1
(0.52)
LTBP3



Citations in the biomedical literature:


Camurati-Engelmann disease
TGFB1
Oligodontia
AXIN2 EDA EDARADD FGFR1 IRF6 LTBP3
MSX1 PAX9 TGFA WNT10A



Camurati-Engelmann disease
Oligodontia

Synonym(s):
- Progressive diaphyseal dysplasia

Synonym(s):
- Selective tooth agenesis

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

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

Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: no data available
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: normal
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
1 MeSH reference: D003966
External references:
6 OMIM references -
No MeSH references


COMMON
SIGNS
- Autosomal dominant inheritance


Camurati-Engelmann disease
Oligodontia

Very frequent
- Anomalies of spine, vertebrae and pelvis
- Bone pain
- Cortical anomaly / thick bone cortical layer
- Diaphyseal anomaly
- Dysostosis / chondrodysplasia / osteodysplasia / osteochondrosis / skeletal dysplasia
- Femur anomaly / absence / agenesis / hypoplasia / bifurcation
- Humerus anomaly / absence / agenesis / hypoplasia / congenital humerus varus
- Hyperostosis
- Osteosclerosis / osteopetrosis / bone condensation
- Radius anomaly / absence / agenesis / hypoplasia / abnormal radial ray
- Skull / cranial anomalies
- Ulnar / cubital anomaly / absence / agenesis / hypoplasia / abnormal ulnar / cubital ray

Frequent
- Abnormal gait
- Metaphyseal anomaly
- Muscle hypotrophy / atrophy / dystrophy / agenesis / amyotrophy
- Muscle weakness / flaccidity
- Restricted joint mobility / joint stiffness / ankylosis

Occasional
- Abnormal fat distribution / lipodystrophy
- Acrocyanosis / Raynaud's phenomenon / vasomotor disorders
- Anaemia
- Anorexia
- Ataxia / incoordination / trouble of the equilibrium
- Biological inflammatory syndrome / increased erythrocyte sedimentation rate / CRP
- Bladder and ureter anomalies
- Cardiomyopathy / hypertrophic / dilated
- Delayed dentition / eruption of teeth / lack of eruption of teeth
- Facial dysmorphism
- Facial palsy
- Feeding disorder / dysphagia / swallowing / sucking disorder / esophageal dyskinesia
- Flat foot
- Frontal bossing / prominent forehead
- Genu valgum
- Glaucoma
- Hearing loss / hypoacusia / deafness
- Hepatomegaly / liver enlargement (excluding storage disease)
- Hip dislocation / dysplasia / coxa valga / coxa vara / coxa plana
- Kyphosis
- Late puberty / hypogonadism / hypogenitalism
- Leukopenia / hypoleukocytosis
- Lordosis
- Marfanoid morphotype
- Multiple caries
- Optic nerve anomaly / optic atrophy / anomaly of the papilla
- Proptosis / exophthalmos
- Scoliosis
- Sensitive trouble / deficit
- Speech troubles / aphasia / dysphasia / echolalia / mutism / logorrhea / dysprosodia
- Splenomegaly


Very frequent
- Anodontia / oligodontia / hypodontia
- Complete / partial microdontia
- Face / facial anomalies
- Hypoplastic mandibula / partial absence of the mandibula
- Tooth shape anomaly

Frequent
- Autosomal recessive inheritance
- X-linked recessive inheritance