multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome

Findings

No curated finding names multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Where it sits

A kind of

• multiple congenital anomalies/dysmorphic syndrome

Narrower terms (69)

• 22q11.2 deletion syndrome
• ablepharon macrostomia syndrome
• acromegaloid facial appearance syndrome
• anophthalmia/microphthalmia-esophageal atresia syndrome
• Antley-Bixler syndrome
• arachnodactyly-intellectual disability-dysmorphism syndrome
• autosomal dominant popliteal pterygium syndrome
• autosomal dominant primary microcephaly
• Bosley-Salih-Alorainy syndrome
• Brachymorphism-onychodysplasia-dysphalangism syndrome
• branchiogenic deafness syndrome
• campomelia, Cumming type
• campomelic dysplasia
• Carpenter syndrome
• cerebrocostomandibular syndrome
• Char syndrome
• CHARGE syndrome
• chromosome 1p32-p31 deletion syndrome
• combined immunodeficiency with faciooculoskeletal anomalies
• contractures-developmental delay-Pierre Robin syndrome
• Donnai-Barrow syndrome
• dysmorphism-conductive hearing loss-heart defect syndrome
• Goodman syndrome
• Hennekam-Beemer syndrome
• hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome
• hypertrichotic osteochondrodysplasia Cantu type
• Hypoglossia-hypodactyly syndrome
• hypomandibular faciocranial dysostosis
• isotretinoin-like syndrome
• Kallmann syndrome-heart disease syndrome
• lethal faciocardiomelic dysplasia
• Malan overgrowth syndrome
• Marshall-Smith syndrome
• Meier-Gorlin syndrome
• microgastria-limb reduction defect syndrome
• microphthalmia with limb anomalies
• Mietens syndrome
• Moebius syndrome
• moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome
• Noonan syndrome
• Noonan syndrome-like disorder with loose anagen hair
• occipital horn syndrome
• oculodentodigital dysplasia
• oculotrichoanal syndrome
• Pallister-Hall syndrome
• PHACE syndrome
• polyvalvular heart disease syndrome
• Potocki-Shaffer syndrome
• Prader-Willi syndrome
• Prader-Willi-like syndrome
• Schinzel-Giedion syndrome
• short stature-heart defect-craniofacial anomalies syndrome
• short stature-wormian bones-dextrocardia syndrome
• SHORT syndrome
• Silver-Russell syndrome
• split hand-foot malformation 3
• symptomatic form of Coffin-Lowry syndrome in female carriers
• TELO2-related intellectual disability-neurodevelopmental disorder
• Toriello-Carey syndrome
• ulnar-mammary syndrome
• and 9 more

Resolves to: multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome

Also called

MCA/variable MRmultiple congenital anomalies-variable intellectual disability with or without dysmorphism syndrome