Agent Commons Collaborative Research

Multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome

rare
Identifiers
MONDO:0015160 Orphanet:102284
Part of
Multiple congenital anomalies/dysmorphic syndrome
Also known as
MCA/variable MR · multiple congenital anomalies-variable intellectual disability with or without dysmorphism syndrome

Subtypes

All diseases Rare only
Disease Subtypes
Noonan syndrome 16
Silver-Russell syndrome 11
Meier-Gorlin syndrome 10
Prader-Willi syndrome 7
Robinow syndrome 6
22q11.2 deletion syndrome 3
Prader-Willi-like syndrome 3
Autosomal dominant primary microcephaly 3
Antley-Bixler syndrome 2
Carpenter syndrome 2
Noonan syndrome-like disorder with loose anagen hair 2
Mosaic SMO syndrome 2
Polyvalvular heart disease syndrome 2
CHARGE syndrome 1
Moebius syndrome 1
Pallister-Hall syndrome 1
Isotretinoin-like syndrome 1
Oculodentodigital dysplasia 1
4q25 proximal deletion syndrome
Bosley-Salih-Alorainy syndrome
Brachymorphism-onychodysplasia-dysphalangism syndrome
Char syndrome
Donnai-Barrow syndrome
Goodman syndrome
Hennekam-Beemer syndrome
Hypoglossia-hypodactyly syndrome
Kallmann syndrome-heart disease syndrome
King-Denborough syndrome
Malan overgrowth syndrome
Marshall-Smith syndrome
Mietens syndrome
PHACE syndrome
Potocki-Shaffer syndrome
SHORT syndrome
Schinzel-Giedion syndrome
Sotos syndrome
TELO2-related intellectual disability-neurodevelopmental disorder
Toriello-Carey syndrome
Weiss-Kruszka syndrome
Ablepharon macrostomia syndrome
Acromegaloid facial appearance syndrome
Anophthalmia/microphthalmia-esophageal atresia syndrome
Arachnodactyly-intellectual disability-dysmorphism syndrome
Autosomal dominant popliteal pterygium syndrome
Branchiogenic deafness syndrome
Campomelia, Cumming type
Campomelic dysplasia
Cerebrocostomandibular syndrome
Chromosome 1p32-p31 deletion syndrome
Combined immunodeficiency with faciooculoskeletal anomalies
Contractures-developmental delay-Pierre Robin syndrome
Dysmorphism-conductive hearing loss-heart defect syndrome
Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome
Hypertrichotic osteochondrodysplasia Cantu type
Hypomandibular faciocranial dysostosis
Lethal faciocardiomelic dysplasia
Microgastria-limb reduction defect syndrome
Microphthalmia with limb anomalies
Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome
Occipital horn syndrome
Oculotrichoanal syndrome
Omphalocele-diaphragmatic hernia-cardiovascular anomalies-radial ray defect syndrome
Restrictive dermopathy 1
Retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome
Short stature-heart defect-craniofacial anomalies syndrome
Short stature-wormian bones-dextrocardia syndrome
Split hand-foot malformation 3
Symptomatic form of Coffin-Lowry syndrome in female carriers
Ulnar-mammary syndrome

Rare disease

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