Select Entries from OMIM --Online Mendelian Inheritance in
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Abnormalities
19 entries found, searching for "microtia"
*251800
MICROTIA WITH MEATAL ATRESIA AND CONDUCTIVE DEAFNESS
*600674
MICROTIA-ANOTIA
*239800
HYPERTELORISM, MICROTIA, FACIAL CLEFTING SYNDROME
*224690
EAR, PATELLA, SHORT STATURE SYNDROME
248910 MASTOCYTOSIS, CUTANEOUS, WITH SHORT STATURE, CONDUCTIVE
HEARING LOSS AND MICROTIA
243440 ISOTRETINOIN EMBRYOPATHY-LIKE SYNDROME
*236670
WALKER-WARBURG SYNDROME
147770 JOHNSON NEUROECTODERMAL SYNDROME
164210 OCULOAURICULOVERTEBRAL DYSPLASIA
#107480
TOWNES-BROCKS SYNDROME; TBS
141400 HEMIFACIAL MICROSOMIA WITH RADIAL DEFECTS
122780 COXOAURICULAR SYNDROME
*154500
TREACHER COLLINS-FRANCESCHETTI SYNDROME 1; TCOF1
154400 ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1
*148900
KLIPPEL-FEIL SYNDROME
*142961
HOMEO BOX B6; HOXB6
#220700
DEAFNESS, AUTOSOMAL RECESSIVE
*314390
VACTERL ASSOCIATION WITH HYDROCEPHALUS, X-LINKED
165680 OSSICULAR MALFORMATIONS, FAMILIAL