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1 OMIM reference -
1 associated gene
24 signs/symptoms
PROTEIN INTERACTIONS: 1
COMMON SIGNS: 7
2 OMIM references -
1 associated gene
86 signs/symptoms
Otopalatodigital syndrome type 1
Oculodentodigital dysplasia

FLNA GJA1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
FLNA
(0.63)
GJA1



Citations in the biomedical literature:


Otopalatodigital syndrome type 1
FLNA
Oculodentodigital dysplasia
GJA1



Otopalatodigital syndrome type 1
Oculodentodigital dysplasia

Synonym(s):
(no synonyms)

Synonym(s):
- Meyer-Schwickerath syndrome
- ODDD syndrome
- Oculodentoosseous dysplasia

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

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

Epidemiological data:
Class of prevalence: -
Average age onset: -
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:
2 OMIM references -
No MeSH references


COMMON
SIGNS
- Anodontia / oligodontia / hypodontia
- Cleft palate without cleft lip / submucosal cleft palate / bifid uvula
- Dense / thickened skull / calvarium / cranial / facial hyperostosis
- Hearing loss / hypoacusia / deafness
- Hypertelorism
- Short big toe
- Short hand / brachydactyly


Otopalatodigital syndrome type 1
Oculodentodigital dysplasia

Very frequent
- Broad nose / nasal bridge
- Downslanted palpebral fissures / anti-mongoloid slanting palpebral fissures
- Prominent supraorbital ridge
- Restricted joint mobility / joint stiffness / ankylosis
- Wide space between 1st-2nd toes
- X-linked recessive inheritance

Frequent
- Bowed diaphysis / diaphyses / long bones
- Elbow dislocation
- Frontal sinus agenesis / anomaly
- Metacarpal anomalies / Archibald's sign
- Osteosclerosis / osteopetrosis / bone condensation
- Proximally set thumb
- Terminal / third phalangeal bone of fingers hypoplasia
- Thumb hypoplasia / aplasia / absence

Occasional
- Anomalies of spine, vertebrae and pelvis
- Carpal bones fusion / synostosis
- Tarsal anomaly / fusion / synostosis


Very frequent
- Anomalies of nose and olfaction
- Anophthalmos / anophthalmia / microphthalmos / microphthalmia
- Anteverted nares / nostrils
- Autosomal dominant inheritance
- Camptodactyly of some fingers
- Clinodactyly of fifth finger
- Enamel anomaly
- Microcornea
- Multiple caries
- Narrow nasal bridge
- Premature lost of decidious teeth
- Syndactyly of fingers / interdigital palm
- Syndactyly of toes
- Thick columella
- Thin / hypoplastic ala nasi

Frequent
- Abnormal fingernails
- Abnormal gait
- Abnormal hair texture / hair dysplasia
- Anomalies of eyes and vision
- Ataxia / incoordination / trouble of the equilibrium
- Bladder and ureter anomalies
- Broad alveolar ridge
- Camptodactyly of fingers
- Cataract / lens opacification
- Cerebellum / cerebellar vermis anomaly / agenesis / hypoplasia
- Clinodactyly of fingers 1,2,3,4 / overlapping fingers
- Conductive deafness / hearing loss
- Cortical anomaly / thick bone cortical layer
- Elocution disorders / dysarthria / dysphonia
- Enlargment of jaw / large jaw
- External ear anomalies
- Glaucoma
- Hemiplegia / diplegia / hemiparesia / limb palsy
- High forehead
- Hypereflexia
- Hypermetropia
- Hyperostosis
- Hypertonia / spasticity / rigidity / stiffness
- Hypotelorism
- Hypotrichosis / atrichia / atrichiasis / scalp hairlessness
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Intracranial / cerebral calcifications
- Median cleft lip
- Metaphyseal anomaly
- Muscle weakness / flaccidity
- Myopia
- Nails anomalies
- Optic nerve anomaly / optic atrophy / anomaly of the papilla
- Prognathism / prognathia
- Seizures / epilepsy / absences / spasms / status epilepticus
- Short / small nose
- slow growth of the hair
- Small / triangular nares / nostrils
- Visual loss / blindness / amblyopia

Occasional
- Abnormal vertebral size / shape
- Aniridia / iris hypoplasia
- Autosomal recessive inheritance
- Blepharophimosis / short palpebral fissures
- Brittle hair / distrix / trichorrhexis
- Cardiac rhythm disorder / arrhythmia
- Clavicle absent / abnormal
- Congenital cardiac anomaly / malformation / cardiopathy
- Deepset eyes / enophthalmos
- Diaphyseal anomaly
- Epicanthic folds
- Fine hair
- Hypoglycemia
- Lateral cleft lip / gingival cleft / paramedian nasal cleft
- Madelung's deformity
- Micrognathia / retrognathia / micrognathism / retrognathism
- Nystagmus
- Palmoplantar hyperkeratosis / keratoderma
- Preaxial polydactyly (hand)
- Strabismus / squint
- Taurodontia
- Umbilical hernia
- Upper limb polydactyly / hexadactyly
- Upslanted palpebral fissures / mongoloid slanting palpebral fissures
- Ventricular septal defect / interventricular communication