multiple congenital anomalies/dysmorphic syndrome without intellectual disability

Findings

No curated finding names multiple congenital anomalies/dysmorphic syndrome without intellectual disability 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 (168)

• 3-M syndrome
• Aase-Smith syndrome
• Ackerman syndrome
• acro-renal-mandibular syndrome
• acrocraniofacial dysostosis
• acrofacial dysostosis, Weyers type
• acrorenal syndrome
• Alagille syndrome
• alar cartilages hypoplasia-coloboma-telecanthus syndrome
• Ascher syndrome
• autosomal dominant prognathism
• Barber-Say syndrome
• Beare-Stevenson cutis gyrata syndrome
• Beemer-Ertbruggen syndrome
• Bencze syndrome
• Binder syndrome
• blepharocheilodontic syndrome
• blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome
• brachytelephalangy-dysmorphism-Kallmann syndrome
• branchio-oto-renal syndrome
• branchiooculofacial syndrome
• camptodactyly syndrome, Guadalajara type 1
• cataract-aberrant oral frenula-growth delay syndrome
• cherubism
• cleft palate-lateral synechia syndrome
• Cooper-Jabs syndrome
• craniofacial-deafness-hand syndrome
• cryptomicrotia-brachydactyly-excess fingertip arch syndrome
• Cyprus facial-neuromusculoskeletal syndrome
• Czeizel-Losonci syndrome
• deafness-craniofacial syndrome
• external auditory canal atresia-vertical talus-hypertelorism syndrome
• femoral-facial syndrome
• fetal akinesia deformation sequence
• flat face-microstomia-ear anomaly syndrome
• Freeman-Sheldon syndrome
• Gordon syndrome
• hand-foot-genital syndrome
• Holt-Oram syndrome
• LADD syndrome
• Marshall syndrome
• median nodule of the upper lip
• microcephaly-albinism-digital anomalies syndrome
• mullerian duct anomalies-limb anomalies syndrome
• multinodular goiter-cystic kidney-polydactyly syndrome
• Nager acrofacial dysostosis
• nasopalpebral lipoma-coloboma syndrome
• Noonan syndrome with multiple lentigines
• oculoauriculovertebral spectrum with radial defects
• otospondylomegaepiphyseal dysplasia, autosomal dominant
• PAGOD syndrome
• posterior fusion of lumbosacral vertebrae-blepharoptosis syndrome
• radial hypoplasia-triphalangeal thumbs-hypospadias-maxillary diastema syndrome
• scalp-ear-nipple syndrome
• Schilbach-Rott syndrome
• short stature-craniofacial anomalies-genital hypoplasia syndrome
• short stature-valvular heart disease-characteristic facies syndrome
• Townes-Brocks syndrome
• Treacher-Collins syndrome
• ventricular extrasystoles with syncopal episodes-perodactyly-robin sequence syndrome
• and 108 more

Resolves to: multiple congenital anomalies/dysmorphic syndrome without intellectual disability

Also called

MCA without intellectual disabilitymultiple congenital anomalies without intellectual disability with or without dysmorphism