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multiple congenital anomalies/dysmorphic syndrome-intellectual disability
Subclasses
Kaufman oculocerebrofacial syndrome
? TBD
Medical condition
syndromic X-linked intellectual disability Shashi type
? TBD
syndromic X-linked intellectual disability characterized by moderate intellectual deficit, obesity, macroorchidism and a characteristic facies that has material basis in mutation in the RBMX gene on chromosome Xq26
Mowat–Wilson syndrome
? TBD
Rare autosomal dominant genetic disorder
syndromic X-linked intellectual disability 7
? TBD
syndromic X-linked intellectual disability characterized by intellectual deficit, obesity, hypogonadism, and tapering fingers that has material basis in variation in the chromosome region Xp11.3-q22
Christianson syndrome
? TBD
Medical condition
Bohring–Opitz syndrome
? TBD
Medical condition
Biemond syndrome
? TBD
Medical condition
Tatton-Brown–Rahman syndrome
? TBD
Overgrowth syndrome caused by DNMT3A gene mutation
Williams syndrome
? TBD
Genetic disorder
Smith–Magenis syndrome
? TBD
Human disease
Börjeson–Forssman–Lehmann syndrome
? TBD
Medical condition
Smith–Lemli–Opitz syndrome
? TBD
Recessive genetic condition
Hirsutism-skeletal dysplasia-intellectual disability syndrome
? TBD
human disease
Cohen syndrome
? TBD
Medical condition
Severe intellectual disability-progressive spastic diplegia syndrome
? TBD
Medical condition
Weaver syndrome
? TBD
Rare genetic overgrowth disorder
Peters-plus syndrome
? TBD
Medical condition
ADNP syndrome
? TBD
Genetic disorder characterized by developmental delay and autistic features
Costello syndrome
? TBD
Medical condition