From: Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
SYNDROME | INHERITANCE | MIM |
---|---|---|
Alopecia-Skeletal anomalies-Mental retardation | Autosomal recessive | 203550 |
Dermotrichic | X-linked recessive | 308205 |
Ectodermal dysplasia-Alopecia-Mental retardation | Autosomal recessive | 203550 |
Hay-Wells syndrome | Autosomal dominant | 106260 |
Hayden syndrome | Uncertain | Reference 24 |
Hereditary mucoepithelial dysplasia | Autosomal dominant | 158310 |
IFAP | X-linked | 308205 |
Ichthyotis-Hypotrichosis-Hypohidrosis | Autosomal recessive | 602400 |
Keratitis-Ichthyosis-Deafness (KID) | Autosomal dominant | 242150 |
Keratosis follicularis spinulosa decalvans | X-linked | 308800 |
Ichthyosis, alopecia, eclabion, ectropion and mental retardation | Autosomal recessive | 242510 |
Trichooculodermovertebral syndrome | Uncertain | 601701 |
Woodhouse-Sakati syndrome | Autosomal recessive | 241080 |