ICD-10: O35.1
Maternal care for (suspected) chromosomal abnormality in fetus
Subcategories
O35.14
Maternal care for (suspected) chromosomal abnormality in fetus, Turner Syndrome
O35.10
Maternal care for (suspected) chromosomal abnormality in fetus, unspecified
O35.19
Maternal care for (suspected) chromosomal abnormality in fetus, other chromosomal abnormality
O35.15
Maternal care for (suspected) chromosomal abnormality in fetus, sex chromosome abnormality
O35.11
Maternal care for (suspected) chromosomal abnormality in fetus, Trisomy 13
O35.12
Maternal care for (suspected) chromosomal abnormality in fetus, Trisomy 18
O35.13
Maternal care for (suspected) chromosomal abnormality in fetus, Trisomy 21
Related Diseases
MEDNIK syndrome
Mowat-Wilson syndrome
Barber-Say syndrome
Ritscher-Schinzel syndrome
Ritscher-Schinzel syndrome 2
3MC syndrome 2
Yunis-Varon syndrome
syndromic X-linked intellectual disability 5
syndromic X-linked intellectual disability Hedera type
syndromic X-linked intellectual disability 7
Wilson-Turner syndrome
chromosome 17p13.1 deletion syndrome
chromosome 18p deletion syndrome
chromosome 19q13.11 deletion syndrome
chromosome 22q11.2 deletion syndrome, distal
chromosome 2p12-p11.2 deletion syndrome
chromosome 2q31.2 deletion syndrome
chromosome 3q13.31 deletion syndrome
chromosome 3q29 microdeletion syndrome
chromosome 4q21 deletion syndrome
chromosome 6q24-q25 deletion syndrome
chromosomal duplication syndrome
chromosome 17q21.31 duplication syndrome
chromosome 2q31.1 duplication syndrome
chromosome 3q29 microduplication syndrome
Loeys-Dietz syndrome
Alstrom syndrome
obsolete Majewski syndrome
Allan-Herndon-Dudley syndrome
obsolete anonychia congenita
Bowen-Conradi syndrome
Perrault syndrome
MASA syndrome
Ohdo syndrome
microcephaly with or without chorioretinopathy, lymphedema, or mental retardation
orofaciodigital syndrome VII
orofaciodigital syndrome IX
chromosome 14q11-q22 deletion syndrome
chromosome 15q25 deletion syndrome
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