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Frontometaphyseal dysplasia

1 OMIM reference -
1 associated gene
33 signs/symptoms

PROTEIN INTERACTIONS: 2

Fetal and neonatal alloimmune thrombocytopenia

6 associated genes
No signs/symptoms info

Frontometaphyseal dysplasia

Fetal and neonatal alloimmune thrombocytopenia

FLNA	(UniProt - OMIM)		CD109	(UniProt - OMIM)
			GP1BA	(UniProt - OMIM)
			GP1BB	(UniProt - OMIM)
			ITGA2	(UniProt - OMIM)
			ITGA2B	(UniProt - OMIM)
			ITGB3	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FLNA FLNA	(0.73) (0.63)	GP1BA ITGB3

Citations in the biomedical literature:

Frontometaphyseal dysplasia		Fetal and neonatal alloimmune thrombocytopenia
	Synonym(s): (no synonyms)		Synonym(s): - NAIT

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

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Certain conditions originating in the perinatal period -

	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: (no data available)

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

Frontometaphyseal dysplasia
	Very frequent - Bowed diaphysis / diaphyses / long bones - Camptodactyly of fingers - Dense / thickened skull / calvarium / cranial / facial hyperostosis - Diaphyseal anomaly - Downslanted palpebral fissures / anti-mongoloid slanting palpebral fissures - Frontal sinus agenesis / anomaly - Hypertelorism - Metaphyseal anomaly - Micrognathia / retrognathia / micrognathism / retrognathism - Prominent supraorbital ridge - Restricted joint mobility / joint stiffness / ankylosis - Tooth shape anomaly - X-linked recessive inheritance Frequent - Abnormal vertebral size / shape - Advanced bone age - Carpal bones fusion / synostosis - Conductive deafness / hearing loss - Elbow dislocation - High vaulted / narrow palate - Long hand / arachnodactyly - Muscle hypotrophy / atrophy / dystrophy / agenesis / amyotrophy - Scoliosis - Sensorineural deafness / hearing loss - Thumb hypoplasia / aplasia / absence - 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
Fetal and neonatal alloimmune thrombocytopenia
(no data available)