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Up to: Multiple congenital anomalies/dysmorphic syndrome

Multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome

0 trials tagged with this condition →

Prader-Willi syndrome 31 trials Sub-types →
Noonan syndrome 21 trials · 24 incl. sub-types Sub-types →
22q11.2 deletion syndrome 7 trials · 13 incl. sub-types Sub-types →
Silver-Russell syndrome 7 trials Sub-types →
CHARGE syndrome 4 trials Sub-types →
Anophthalmia/microphthalmia-esophageal atresia syndrome 4 trials
Antley-Bixler syndrome 2 trials Sub-types →
Mobius syndrome 2 trials Sub-types →
PHACE syndrome 2 trials
Pallister-Hall syndrome 0 trials · 2 incl. sub-types Sub-types →
Meier-Gorlin syndrome 1 trial Sub-types →
Sotos syndrome 1 trial
Occipital horn syndrome 1 trial
Split hand-foot malformation 3 1 trial
4q25 proximal deletion syndrome 0 trials
Bosley-Salih-Alorainy syndrome 0 trials
Brachymorphism-onychodysplasia-dysphalangism syndrome 0 trials
Carpenter syndrome 0 trials Sub-types →
Char syndrome 0 trials
Donnai-Barrow syndrome 0 trials
Goodman syndrome 0 trials
Hennekam-Beemer syndrome 0 trials
Hypoglossia-hypodactyly syndrome 0 trials
Kallmann syndrome-heart disease syndrome 0 trials
King-Denborough syndrome 0 trials
Malan overgrowth syndrome 0 trials
Marshall-Smith syndrome 0 trials
Mietens syndrome 0 trials
Noonan syndrome-like disorder with loose anagen hair 0 trials Sub-types →
Potocki-Shaffer syndrome 0 trials
Prader-Willi-like syndrome 0 trials Sub-types →
Robinow syndrome 0 trials Sub-types →
SHORT syndrome 0 trials
Schinzel-Giedion syndrome 0 trials
TELO2-related intellectual disability-neurodevelopmental disorder 0 trials
Toriello-Carey syndrome 0 trials
Weiss-Kruszka syndrome 0 trials
Ablepharon macrostomia syndrome 0 trials
Acromegaloid facial appearance syndrome 0 trials
Arachnodactyly-intellectual disability-dysmorphism syndrome 0 trials
Autosomal dominant popliteal pterygium syndrome 0 trials
Autosomal dominant primary microcephaly 0 trials Sub-types →
Branchiogenic deafness syndrome 0 trials
Campomelia, Cumming type 0 trials
Campomelic dysplasia 0 trials
Cerebrocostomandibular syndrome 0 trials
Chromosome 1p32-p31 deletion syndrome 0 trials
Combined immunodeficiency with faciooculoskeletal anomalies 0 trials
Contractures-developmental delay-Pierre Robin syndrome 0 trials
Dysmorphism-conductive hearing loss-heart defect syndrome 0 trials
Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome 0 trials
Hypertrichotic osteochondrodysplasia Cantu type 0 trials
Hypomandibular faciocranial dysostosis 0 trials
Isotretinoin-like syndrome 0 trials Sub-types →
Lethal faciocardiomelic dysplasia 0 trials
Microgastria-limb reduction defect syndrome 0 trials
Microphthalmia with limb anomalies 0 trials
Mosaic SMO syndrome 0 trials Sub-types →
Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome 0 trials
Oculodentodigital dysplasia 0 trials Sub-types →
Oculotrichoanal syndrome 0 trials
Omphalocele-diaphragmatic hernia-cardiovascular anomalies-radial ray defect syndrome 0 trials
Polyvalvular heart disease syndrome 0 trials Sub-types →
Restrictive dermopathy 1 0 trials
Retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome 0 trials
Short stature-heart defect-craniofacial anomalies syndrome 0 trials
Short stature-wormian bones-dextrocardia syndrome 0 trials
Symptomatic form of Coffin-Lowry syndrome in female carriers 0 trials
Ulnar-mammary syndrome 0 trials