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Matthew-Wood syndrome

2 OMIM references -
2 associated genes
22 signs/symptoms

PROTEIN INTERACTIONS: 1
COMMON SIGNS: 5

Bohring-Opitz syndrome

1 OMIM reference -
1 associated gene
52 signs/symptoms

Matthew-Wood syndrome

Bohring-Opitz syndrome

RARB	(UniProt - OMIM)		ASXL1	(UniProt - OMIM)
STRA6	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	RARB	(0.56)	ASXL1

Citations in the biomedical literature:

Matthew-Wood syndrome		Bohring-Opitz syndrome
	Synonym(s): - Anophthalmia - pulmonary hypoplasia - MCOPS9 - Syndromic microphthalmia type 9		Synonym(s): - BOS syndrome - Bohring syndrome - C-like syndrome - Oberklaid-Danks syndrome - Opitz trigonocephaly-like syndrome

	Classification (Orphanet): - Rare abdominal surgical disease - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic disease - Rare respiratory disease - Rare surgical thoracic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic 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: before age 5 Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: 2 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references


COMMON SIGNS	- Congenital cardiac anomaly / malformation / cardiopathy - Failure to thrive / difficulties for feeding in infancy / growth delay - Intellectual deficit / mental / psychomotor retardation / learning disability - Intrauterine growth retardation - Low set ears / posteriorly rotated ears

Matthew-Wood syndrome		Bohring-Opitz syndrome
	Very frequent - Anophthalmos / anophthalmia / microphthalmos / microphthalmia Frequent - Absent lobe / lung / segmentation defect / abnormal lobulation / sequestration - Diaphragmatic hernia / defect / agenesis - Hypoplastic lungs / pulmonary hypoplasia / agenesis - Stillbirth / neonatal death Occasional - Agenesis / hypoplasia / aplasia of kidneys - Annular pancreas - Asplenia / polysplenia / spleen lobulation / accessory spleen - Autosomal recessive inheritance - Congenital absence / agenesis / aplasia / hypoplasia of the pancreas - Duodenal atresia / stenosis / megaduodenum - Ectopic / horseshoe / fused kidneys - Hypotonia - Larynx / laryngeal stenosis / atresia - Undescended / ectopic testes / cryptorchidia / unfixed testes - Uterine / uterus / Fallopian tubes anomalies - Vesicorenal / vesicoureteral reflux		Very frequent - Beaked nose - Broad cheeks / cherub-like / cherubin face - Broad nose / nasal bridge - Camptodactyly of fingers - Capillary hemangioma / nevus / naevus flammeus / port-wine stain - Cleft palate without cleft lip / submucosal cleft palate / bifid uvula - Coarse / thick hair - Flat supraorbital ridge - Hirsutism / hypertrichosis / Increased body hair - Low hair line-front - Microcephaly - Micrognathia / retrognathia / micrognathism / retrognathism - Narrow forehead - Proptosis / exophthalmos - Restricted joint mobility / joint stiffness / ankylosis - Trigonocephaly - Ulnar deviation of fingers - Upslanted palpebral fissures / mongoloid slanting palpebral fissures Frequent - Abnormally placed nipples - Anomalies of spine, vertebrae and pelvis - Anterior chamber anomaly - Cleft lip - Corpus callosum / septum pellucidum total / partial agenesis - Cortical atrophy without hydrocephaly / cerebral hemiatrophy / subcortical atrophy - Death in infancy - Dilated cerebral ventricles without hydrocephaly - Elbow dislocation - Gastroesophageal reflux / pyrosis / esophagitis / hiatal hernia / gastroparesia - Hypertelorism - Intestinal / gut / bowel malrotation - Narrow rib cage / thorax - Oral synechiae / abnormal frenulae - Retinopathy - Seizures / epilepsy / absences / spasms / status epilepticus - Short rib cage / thorax - Strabismus / squint - Structural anomalies of the pancreas - Supernumerary nipples / polythelia - Synophris / synophrys Occasional - Dandy-Walker anomaly - Hearing loss / hypoacusia / deafness - Inguinal / inguinoscrotal / crural hernia - Myopia - Polyhydramnios - Renal / kidney anomalies - Small foot - Talipes-varus / metatarsal varus