Mondo Disease Ontology
63848 terms(s) returned
| Term Type: | Record: 60451 to 60500 of 63848 Records | Page: 1210 of 1277, First Previous Next Last | Show Records Per Page |
- syndactyly-telecanthus-anogenital and renal malformations syndrome
- syndesmodysplasic dwarfism
- syndesmosis
- syndrome caused by partial chromosomal deletion
- syndrome caused by partial chromosomal duplication
- syndrome caused by partial chromosomal duplication of the short arm of chromosome 9
- syndromic X-linked intellectual disability 12
- syndromic X-linked intellectual disability 14
- syndromic X-linked intellectual disability 17
- syndromic X-linked intellectual disability 34
- syndromic X-linked intellectual disability 5
- syndromic X-linked intellectual disability 7
- syndromic X-linked intellectual disability 94
- syndromic X-linked intellectual disability Abidi type
- syndromic X-linked intellectual disability Chudley-Schwartz type
- syndromic X-linked intellectual disability Claes-Jensen type
- syndromic X-linked intellectual disability Hedera type
- syndromic X-linked intellectual disability Lubs type
- syndromic X-linked intellectual disability Najm type
- syndromic X-linked intellectual disability Nascimento type
- syndromic X-linked intellectual disability Raymond type
- syndromic X-linked intellectual disability Shashi type
- syndromic X-linked intellectual disability Shrimpton type
- syndromic X-linked intellectual disability Siderius type
- syndromic X-linked intellectual disability Snyder type
- syndromic agammaglobulinemia
- syndromic breast hypoplasia/aplasia
- syndromic complex neurodevelopmental disorder
- syndromic congenital heart disease
- syndromic congenital sodium diarrhea
- syndromic constitutional thrombocytopenia
- syndromic craniosynostosis
- syndromic disease
- syndromic disease, non-human animal
- syndromic dyslipidemia
- syndromic intellectual disability
- syndromic lacrimal system disorder
- syndromic microphthalmia
- syndromic microphthalmia type 5
- syndromic microspherophakia
- syndromic multisystem autoimmune disease due to ITCH deficiency
- syndromic oculocutaneous albinism
- syndromic or isolated
- syndromic orbital border hypoplasia
- syndromic recessive X-linked ichthyosis
- syndromic retinal atrophy, BBS2-related, dog
- syndromic retinal atrophy, BBS7-related, Rhesus monkey
- syngamus trachea, non-human animal
- syngnathia multiple anomalies
- syngnathia-cleft palate syndrome
