ODCs

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1 OMIM reference -
1 associated gene
21 signs/symptoms

PROTEIN INTERACTIONS: 1

4 OMIM references -
3 associated genes
1 sign/symptom

Hypoparathyroidism - deafness - renal disease

Congenital diaphragmatic hernia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	GATA3	(0.65)	ZFPM2

Citations in the biomedical literature:

Hypoparathyroidism - deafness - renal disease		Congenital diaphragmatic hernia
	Synonym(s): - Barakat syndrome - HDR syndrome		Synonym(s): - CDH - Diaphragmatic agenesia

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare endocrine disease - Rare genetic disease - Rare otorhinolaryngologic disease - Rare renal disease		Classification (Orphanet): - Rare abdominal surgical disease - Rare developmental defect during embryogenesis - Rare respiratory disease - Rare surgical thoracic 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: childhood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: before age 5 Type of inheritance: multigenic/multifactorial

	External references: 1 OMIM reference - No MeSH references		External references: 4 OMIM references - 1 MeSH reference: C538080

Hypoparathyroidism - deafness - renal disease		Congenital diaphragmatic hernia
	Very frequent - Autosomal dominant inheritance - Hypocalcemia - Hypoparathyroidy - Sensorineural deafness / hearing loss Frequent - Agenesis / hypoplasia / aplasia of kidneys - Contractures / cramps / trismus / tetania / claudication / opisthotonos - Humour troubles / anxiety / depression / apathy / euphoria / irritability - Seizures / epilepsy / absences / spasms / status epilepticus Occasional - Ectopic / horseshoe / fused kidneys - Failure to thrive / difficulties for feeding in infancy / growth delay - Gastric / pyloric stenosis - Hematuria / microhematuria - Multicystic kidney / renal dysplasia - Nystagmus - Proteinuria - Psoriasis - Ptosis - Renal failure - Retinitis pigmentosa / retinal pigmentary changes - Ventricular septal defect / interventricular communication - Vesicorenal / vesicoureteral reflux		Very frequent - Diaphragmatic hernia / defect / agenesis