Phenotypes for disease #05153 (MCPH (microcephaly, primary, autosomal recessive (MCPH)))

8 entries on 1 page. Showing entries 1 - 8.
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Phenotype details     

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Diagnosis/Definite     

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Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000054215 Reduced head circumference (HP:0000252), reduced length (HP:?), low weight (HP:0004325), motor development delay (HP:0001270), loss of speech (HP:0002371) and cognition impairment (HP:0100543), severe muscle wasting (HP:0003202), hypertonia (HP:0001276), brisk deep tendon reflex (HP:0006801), down-slanting eyes (HP:0000494), prominent eyelashes (HP:0011231), thin vermilion of the lips (HP:0011339), exotropia (HP:0000577), undescended testicles (HP:?), type 1 diabetes (HP:0100651), gastrostomy tube (HP:0011471), hypomyelination (HP:0003429), White-matter volume markedly diminished (HP:?), thin corpus callosum (HP:0002079), thin brain stem (HP:0002365) - - Familial, autosomal recessive 11y06m - 00y05m - - Jamie Zeegers 00074397
0000054216 Reduced head circumference (HP:0000252), reduced length (HP:?), low weight (HP:0004325), motor development delay (HP:0001270), loss of speech (HP:0002371) and cognition impairment (HP:0100543), severe muscle wasting (HP:0003202), hypertonia (HP:0001276), brisk deep tendon reflex (HP:0006801), prominent eyelashes (HP:0011231), thin vermilion of the lips (HP:0011339), poor dentition (HP:0000696), malformed teeth (HP:0006482), hypomyelination (HP:0003429), White-matter volume markedly diminished (HP:?), thin corpus callosum (HP:0002079), slightly thin brain stem (HP:0002365) - - Familial, autosomal recessive 10y03m - 00y08m - - Jamie Zeegers 00074398
0000054217 no decreased head circumference at birth (-HP:0011451), Reduced head circumference (HP:0000252), reduced length (HP:?), low weight (HP:0004325), motor development delay (HP:0001270), loss of speech (HP:0002371) and cognition impairment (HP:0100543), severe muscle wasting (HP:0003202), limited range of motion of the hips and knees (HP:?), hyperextensibility of wrists (HP:0005072) and ankles (HP:?), brisk deep tendon reflex (HP:0006801), up-slanting eyes (HP:0000582), bulbous nasal tip (HP:0000414), protuberant ears (HP:?) with hypoplastic antihelix (HP:0009739), large atrial septal defect (HP:0011643), gastrostomy tube (HP:0011471), white-matter volume markedly diminished (HP:?), very thin corpus callosum (HP:0002079), slightly thin brain stem (HP:0002365) - - Familial, autosomal recessive 09y05m - 00y00m - - Jamie Zeegers 00074399
0000054218 decreased head circumference present at birth (HP:0011451), Reduced head circumference (HP:0000252), reduced length (HP:?), low weight (HP:0004325), motor development delay (HP:0001270), loss of speech (HP:0002371) and cognition impairment (HP:0100543), severe muscle wasting (HP:0003202), hyperextensibility of the wrists (HP:0005072) and ankles (HP:?), brisk deep tendon reflex (HP:0006801), down-slanting eyes (HP:0000494), blunted nasal tip (HP:?), prominent jaw (HP:0000303), white-matter volume markedly diminished (HP:?), very thin corpus callosum (HP:0002079), slightly thin brain stem (HP:0002365) - - Familial, autosomal recessive 07y08m - 00y00m - - Jamie Zeegers 00074400
0000143363 Meckel-syndrome 12 Renal agenesis (HP:0000104), Cerebral hypoplasia (HP:0006872), Cerebellar hypoplasia (HP:0001321), Occipital lobe agenesis, Ureteral agenesis (HP:0012300), Hypoplasia of the uterus (HP:0000013) - - Familial, autosomal recessive - - - - - Isabel Filges 00181109
0000290117 see paper; ..., OFC </= -3 SDS; global developmental delay; no/limited (10/10); severe intellectual disability (10/10); autism spectrum disorder (10/10); appendicular spasticity (3/10); no seizures; MRI WM thinning with ventricular dilatation microcephaly NEDMISBA Familial, autosomal recessive - - - - - Johan den Dunnen 00396962
0000294251 see paper; ..., small heads, mild-moderate intellectual disability, short stature, narrow and oval shaped faces, receding foreheads, large ears, prominent nose; attention deficit behavior, speech apraxia; never attended school; affected males spend time wandering streets, no concept of money, not able to perform any conceptual work, recognize relatives, find their way home, sense of self-respect, comfortable with strangers and are friendly microcephaly MCPH5 Familial, autosomal recessive - - - - - Johan den Dunnen 00401208
0000346582 see paper; ..., primary microcephaly, OFC SD<3; mild-moderate intellectual disability; no dysmorphic features, no ocular malformations, no failure to thrive microcephaly MCPH18 Familial, autosomal dominant - - - - - Johan den Dunnen 00458137
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