Select Entries from OMIM -- Online Mendelian Inheritance in
Man
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Abnormalities
32 entries found, searching for "microphthalmos"
*600165
NANOPHTHALMOS 1; NNO1
*251600
MICROPHTHALMOS, AUTOSOMAL RECESSIVE
*152950
LYMPHEDEMA, MICROCEPHALY, CHORIORETINOPATHY SYNDROME
157100 MICROPHTHALMOS, PIGMENTARY RETINOPATHY, AND GLAUCOMA
272550 TACHYCARDIA, HYPERTENSION, MICROPHTHALMOS, AND
HYPERGLYCINURIA
268320 RODRIGUES BLINDNESS
251700 MICROPHTHALMOS WITH HYPERMETROPIA, RETINAL DEGENERATION,
MACROPHAKIA AND DENTAL ANOMALIES
156900 MICROPHTHALMOS WITH MYOPIA AND CORECTOPIA
*251500
MICROPHTHALMIA AND MENTAL DEFICIENCY
*309800
MICROPHTHALMIA OR ANOPHTHALMOS, WITH ASSOCIATED ANOMALIES;
MAA
266400 REESE RETINAL DYSPLASIA
#601547
CATARACT, CONGENITAL, CERULEAN TYPE, 2; CCA2
#180500
RIEGER SYNDROME, TYPE 1; RIEG1
600992 ANOPHTHALMIA AND ESOPHAGEAL ATRESIA
*115660
CATARACT, CONGENITAL, CERULEAN TYPE, 1; CCA1
120433 COLOBOMA, UVEAL, WITH CLEFT LIP AND PALATE AND MENTAL
RETARDATION
*302200
CATARACT, CONGENITAL TOTAL, WITH POSTERIOR SUTURAL OPACITIES IN
HETEROZYGOTES; CCT
*164200
OCULODENTODIGITAL DYSPLASIA; ODDD
*227650
FANCONI ANEMIA, COMPLEMENTATION GROUP A; FANCA
212550 CATARACT, MICROPHTHALMIA, AND NYSTAGMUS
257910 OCULOPALATOCEREBRAL DWARFISM
234100 HALLERMANN-STREIFF SYNDROME; HSS
309700 MICROPHTHALMIA
*206900
ANOPHTHALMOS, TRUE OR PRIMARY
*259700
OSTEOPETROSIS, AUTOSOMAL RECESSIVE
*255800
SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1
*305600
FOCAL DERMAL HYPOPLASIA; DHOF
*211890
CAMPOMELIA, CUMMING TYPE
*310600
NORRIE DISEASE; NDP
*248700
MARDEN-WALKER SYNDROME
*236670
WALKER-WARBURG SYNDROME
*113620
BRANCHIAL CLEFTS WITH CHARACTERISTIC FACIES, GROWTH RETARDATION,
IMPERFORATE NASOLACRIMAL DUCT, AND PREMATURE AGING