Cutaneous mastocytosis-deafness-microtia syndrome
ORPHA:21353M syndrome
ORPHA:2616Albinism-deafness syndrome
ORPHA:998Branchiogenic deafness syndrome
ORPHA:50815Camptodactyly-tall stature-scoliosis-hearing loss syndrome
ORPHA:85164Cataract-ataxia-deafness syndrome
ORPHA:1368Deafness-craniofacial syndrome
ORPHA:3241Deafness-epiphyseal dysplasia-short stature syndrome
ORPHA:3218Deafness-hypogonadism syndrome
ORPHA:90646Deafness-infertility syndrome
ORPHA:94064Deafness-oligodontia syndrome
ORPHA:3230Dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome
ORPHA:71267Dysmorphism-short stature-deafness-difference of sex development syndrome
ORPHA:2282Ear-patella-short stature syndrome
ORPHA:2554Eng-Strom syndrome
ORPHA:1937Generalized resistance to thyroid hormone
ORPHA:3221Hypotrichosis-deafness syndrome
ORPHA:330029Jervell and Lange-Nielsen syndrome
ORPHA:90647Malformation syndrome with short stature
ORPHA:139021Midface hypoplasia-hearing impairment-elliptocytosis-nephrocalcinosis syndrome
ORPHA:688581Myhre syndrome
ORPHA:2588Neutropenia-monocytopenia-deafness syndrome
ORPHA:2690Palmoplantar keratoderma-deafness syndrome
ORPHA:2202Pendred syndrome
ORPHA:705Perrault syndrome
ORPHA:2855Retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome
ORPHA:494439Short stature-deafness-neutrophil dysfunction-dysmorphism syndrome
ORPHA:2866Short stature-webbed neck-heart disease syndrome
ORPHA:2865Spastic paraparesis-deafness syndrome
ORPHA:2815Split hand-split foot-deafness syndrome
ORPHA:71271Subaortic stenosis-short stature syndrome
ORPHA:3191Tietz syndrome
ORPHA:42665Usher syndrome
ORPHA:886X-linked spinocerebellar ataxia type 3
ORPHA:85297