Phenotype #0000230583

Individual ID 00303505
Associated disease ?
Diagnosis/Initial -
Diagnosis/Definite -
Phenotype details postnatal growth deficiency; no developmental delay, no initellectual disability; no seizures; no hypotonia, no contractures; no endocrine issues; no hypothyroidism; no immunodeficiency; normal hands, normal feet; normal skin; pectus; no scoliosis; no inguinal hernia; myocardial insufficiency;; no gastrourigenital defects; no lymphatic malformations; no recurrent infections
Inheritance Familial, autosomal dominant
Age/Examination >18y (later than 18 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Tumor/MSI -
Diagnosis/Criteria -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2020-06-15 09:56:59 +02:00 (CEST)
Date last edited N/A

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