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Malformative pathway
Gallery
androgen insentivity syndrome
bronchopulmonary foregut malformations
extrahepatic biliary tract atresia
holoprosencephalies
lissencephaly type 1
Meckel syndrome
monosomy X
multiple intestinal atresias
multiple intestinal atresias syndrome
non-syndromic BNOMRD
omphalocele with absent radial ray complex
radial ray defects
Smith-Lemli-Opitz syndrome
thanatophoric dysplasias
trisomy 13
tuberous sclerosis
Index
Show all
A
Adams-Oliver syndrome
Alagille disease
Alstrom syndrome
androgen insentivity syndrome
autosomal recessive microtia
B
blepharophimosis, ptosis, and epicanthus inversus syndrome
bronchopulmonary foregut malformations
C
cerebrooculofacioskeletal syndrome type 4
CHARGE association
Cohen syndrome
Cumming syndrome
D
developmental programmed cell death
diabetic embryopathy
E
Elejalde disease
extrahepatic biliary tract atresia
F
familial megacalyces
Feingold syndrome
Frasier syndrome
G
Goldenhar syndrome
Greig cephalopolysyndactyly syndrome
H
high forehead
holoprosencephalies
hydrolethalus syndrome
I
Ivemark syndrome
K
Kartagener syndrome
Kozlowski type of spondylometaphyseal dysplasia
L
limb deficiency defects
lissencephaly type 1
M
Martinez-Frias syndrome
Meckel syndrome
monosomy X
multiple intestinal atresias
multiple intestinal atresias syndrome
N
NKX2E
non-syndromic BNOMRD
O
oculo-auricular syndrome
omphalocele with absent radial ray complex
orofaciodigital syndrome type 2
oromandibular-limb hypogenesis
otopalatodigital syndrome type 2
P
panlobar nephroblastomatosis
partial deletion of 21q22.2-q22.3
R
radial ray defects
RAPADILINO syndrome
rhizomelic limbs
right atrial isomerism
S
Saethre-Chotzen syndrome
SC phocomelia syndrome
Schinzel phocomelia syndrome
Simpson-Golabi-Behmel syndrome
SITCDKP syndrome
skeletal development
Smith-Lemli-Opitz syndrome
split-hand/foot malformation with long bone deficiencies
spondylocostal dysostosis
T
Teebi syndrome
thanatophoric dysplasias
thin upper lip
trisomy 13
tuberous sclerosis
V
Van der Woude syndrome
VATER association
W
Walker-Warburg syndrome
X
X-linked cleft palate with ankyloglossia
X-linked dominant chondrodysplasia punctata type 2
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