UNSW Embryology
COELOMIC CAVITY AND ITS DERIVATIVES
DIAPHRAGMATIC HERNIA
Select Entries from OMIM |
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This page is for computers without external internet access. Normally the blue numbers below would link to a full description of the abnormality. |
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33 entries found, searching for "diaphragmatic
hernia" 142340 HERNIA, DIAPHRAGMATIC *229850 FRYNS SYNDROME; FRNS 306950 HERNIA, ANTERIOR DIAPHRAGMATIC 222448 DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM, MYOPIA, AND SENSORINEURAL DEAFNESS 226735 EPIDERMOLYSIS BULLOSA WITH DIAPHRAGMATIC HERNIA 222400 DIAPHRAGM, UNILATERAL AGENESIS OF 223330 DIVERTICULOSIS OF BOWEL, HERNIA, AND RETINAL DETACHMENT 122470 CORNELIA DE LANGE SYNDROME 1; CDL1 #312870 SIMPSON DYSMORPHIA SYNDROME; SDYS #194080 WILMS TUMOR AND PSEUDOHERMAPHRODITISM *313850 THORACOABDOMINAL SYNDROME; THAS #130000 EHLERS-DANLOS SYNDROME, TYPE I; EDS1 *110100 BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS; BPES *267000 RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM *169400 PELGER-HUET ANOMALY *206500 ANENCEPHALY #194190 WOLF-HIRSCHHORN SYNDROME; WHS *179820 RENIN; REN *309801 MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS *134770 FERRITIN HEAVY CHAIN 1; FTH1 *304110 CRANIOFRONTONASAL SYNDROME; CFNS *305600 FOCAL DERMAL HYPOPLASIA; DHOF *150240 LAMININ, BETA-1; LAMB1 *219100 CUTIS LAXA 202660 AGONADISM WITH MULTIPLE INTERNAL MALFORMATIONS #215100 RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1 265430 PULMONARY HYPOPLASIA *276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY *245600 LARSEN SYNDROME, RECESSIVE *211750 C SYNDROME 122920 CRANIOFRONTAL DYSPLASIA 601165 CLEFT LIP/PALATE WITH CHARACTERISTIC FACIES, INTESTINAL MALROTATION, AND LETHAL CONGENITAL HEART DISEASE #601803 PALLISTER-KILLIAN SYNDROME; PKS |
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