Poor growth, postnatal
Symptom Information:
Symptom ID: | OMIM : No Id available | ||
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Database Frequency: | 8 / 7739 | ||
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All diseases associated with this symptom:
15q24 microdeletion syndrome | (Orphanet:94065) |
ALDH18A1-related De Barsy syndrome | (Orphanet:35664) |
Autosomal recessive cutis laxa type 2B | (Orphanet:357064) |
KEPPEN-LUBINSKY SYNDROME | (OMIM:614098) |
PONTOCEREBELLAR HYPOPLASIA, TYPE 1B | (OMIM:614678) |
Pontocerebellar hypoplasia type 8 | (Orphanet:324569) |
Renal tubulopathy - encephalopathy - liver failure | (Orphanet:254902) |
Wiedemann-Rautenstrauch syndrome | (Orphanet:3455) |