ODCs

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1 OMIM reference -
1 associated gene
33 signs/symptoms

COMMON GENES: 1
COMMON SIGNS: 11

1 OMIM reference -
1 associated gene
24 signs/symptoms

Frontometaphyseal dysplasia

Otopalatodigital syndrome type 1

FLNA

Citations in the biomedical literature:

Frontometaphyseal dysplasia		Otopalatodigital syndrome type 1

	Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease		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 (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: - Type of inheritance: x-linked dominant		Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: x-linked dominant

	External references: 1 OMIM reference - 1 MeSH reference: C538064		External references: 1 OMIM reference - No MeSH references


COMMON SIGNS	- Bowed diaphysis / diaphyses / long bones - Carpal bones fusion / synostosis - Dense / thickened skull / calvarium / cranial / facial hyperostosis - Downslanted palpebral fissures / anti-mongoloid slanting palpebral fissures - Elbow dislocation - Frontal sinus agenesis / anomaly - Hypertelorism - Prominent supraorbital ridge - Restricted joint mobility / joint stiffness / ankylosis - Thumb hypoplasia / aplasia / absence - X-linked recessive inheritance

Frontometaphyseal dysplasia		Otopalatodigital syndrome type 1
	Very frequent - Camptodactyly of fingers - Diaphyseal anomaly - Metaphyseal anomaly - Micrognathia / retrognathia / micrognathism / retrognathism - Tooth shape anomaly Frequent - Abnormal vertebral size / shape - Advanced bone age - Conductive deafness / hearing loss - High vaulted / narrow palate - Long hand / arachnodactyly - Muscle hypotrophy / atrophy / dystrophy / agenesis / amyotrophy - Scoliosis - Sensorineural deafness / hearing loss - Ulnar deviation of fingers Occasional - Atrioventricular canal - Autosomal dominant inheritance - Craniostenosis / craniosynostosis / sutural synostosis - Larynx / laryngeal stenosis / atresia - Megaureter / hydronephrosis / pyeloureteral junction syndrome - Tracheal atresia / stenosis - Ureteral stenosis / narrowing - Urethral anomalies / stenosis / posterior urethral valves / megalocystis		Very frequent - Anodontia / oligodontia / hypodontia - Broad nose / nasal bridge - Cleft palate without cleft lip / submucosal cleft palate / bifid uvula - Hearing loss / hypoacusia / deafness - Short big toe - Wide space between 1st-2nd toes Frequent - Metacarpal anomalies / Archibald's sign - Osteosclerosis / osteopetrosis / bone condensation - Proximally set thumb - Short hand / brachydactyly - Terminal / third phalangeal bone of fingers hypoplasia Occasional - Anomalies of spine, vertebrae and pelvis - Tarsal anomaly / fusion / synostosis